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dbVar

Database of genomic structural variation

esv1631266

Organism: Homo sapiens

Study:estd22 (Levy et al. 2007)
Variant Type:inversion
Method Type:Sequencing
Submitted on:NCBI36 (hg18)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:4,064

Publication(s):Levy et al. 2007

Links to Other Resources

Overlapping Genes

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: 158 SVs from 41 studies. See in: genome view

Remapped(Score: Perfect):107,418,627-107,422,690

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv1631266	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	107,418,627	107,422,690
esv1631266	Remapped	Pass	GRCh38.p12	PATCHES	Second Pass	NW_017852930.1	Chr7\|NW_01 7852930.1	264,267	267,973
esv1631266	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	107,059,072	107,063,135
esv1631266	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000007.12	Chr7	106,846,308	106,850,371

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
essv3902601	inversion	HuRef	Sequencing	Sequence alignment	780,358

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv3902601	Remapped	Pass	NW_017852930.1:g.2 64267_267973inv	GRCh38.p12	Second Pass	NW_017852930.1	Chr7\|NW_01 7852930.1	264,267	267,973
essv3902601	Remapped	Perfect	NC_000007.14:g.107 418627_107422690in v	GRCh38.p12	First Pass	NC_000007.14	Chr7	107,418,627	107,422,690
essv3902601	Remapped	Perfect	NC_000007.13:g.107 059072_107063135in v	GRCh37.p13	First Pass	NC_000007.13	Chr7	107,059,072	107,063,135
essv3902601	Submitted genomic		NC_000007.12:g.106 846308_106850371in v	NCBI36 (hg18)		NC_000007.12	Chr7	106,846,308	106,850,371

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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