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dbVar

Database of genomic structural variation

esv3814863

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:
Chr6:g.(35514168_35516168)_chr8:(123613582_123615582)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: 148 SVs from 43 studies. See in: genome view

Remapped(Score: Perfect):35,546,391-35,548,391

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
esv3814863	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	35,546,391	35,548,391	35,546,391	35,548,391
esv3814863	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	122,601,343	122,603,343	122,601,343	122,603,343
esv3814863	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000006.11	Chr6	35,514,168	35,516,168	35,514,168	35,516,168
esv3814863	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000008.10	Chr8	123,613,582	123,615,582	123,613,582	123,615,582

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
essv16644702	interchromosomal translocation	2120208	Curated	Curated	66

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop	strand
essv16644702	Remapped	Perfect	GRCh38.p12	First Pass	NC_000006.12	Chr6	35,546,391	35,548,391	35,546,391	35,548,391	not reported
essv16644702	Remapped	Perfect	GRCh38.p12	First Pass	NC_000008.11	Chr8	122,601,343	122,603,343	122,601,343	122,603,343	not reported
essv16644702	Submitted genomic		GRCh37 (hg19)		NC_000006.11	Chr6	35,514,168	35,516,168	35,514,168	35,516,168	not reported
essv16644702	Submitted genomic		GRCh37 (hg19)		NC_000008.10	Chr8	123,613,582	123,615,582	123,613,582	123,615,582	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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