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dbVar

Database of genomic structural variation

esv3796494

Organism: Homo sapiens

Study:estd192 (COSMIC)
Variant Type:complex chromosomal rearrangement
Method Type:Curated
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:2,001

Description:Chr14:g.(38206314_38208314)_chr6:(140594601_14
0596601)bkpt
Publication(s):Forbes et al. 2008, Forbes et al. 2008

Links to Other Resources

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 82 SVs from 20 studies. See in: genome view

Remapped(Score: Perfect):140,273,464-140,275,464

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
esv3796494	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	140,273,464	140,275,464	140,273,464	140,275,464
esv3796494	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000014.9	Chr14	37,737,109	37,739,109	37,737,109	37,739,109
esv3796494	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000006.11	Chr6	140,594,601	140,596,601	140,594,601	140,596,601
esv3796494	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000014.8	Chr14	38,206,314	38,208,314	38,206,314	38,208,314

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
essv16624177	interchromosomal translocation	2120206	Curated	Curated	25

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop	strand
essv16624177	Remapped	Perfect	GRCh38.p12	First Pass	NC_000006.12	Chr6	140,273,464	140,275,464	140,273,464	140,275,464	not reported
essv16624177	Remapped	Perfect	GRCh38.p12	First Pass	NC_000014.9	Chr14	37,737,109	37,739,109	37,737,109	37,739,109	not reported
essv16624177	Submitted genomic		GRCh37 (hg19)		NC_000006.11	Chr6	140,594,601	140,596,601	140,594,601	140,596,601	not reported
essv16624177	Submitted genomic		GRCh37 (hg19)		NC_000014.8	Chr14	38,206,314	38,208,314	38,206,314	38,208,314	not reported

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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