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dbVar

Database of genomic structural variation

esv1505928

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:10,056

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

Remapped(Score: Pass):47,306,914-47,316,969

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv1505928	Remapped	Pass	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	47,306,914	47,316,969
esv1505928	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	48,214,931	48,226,228
esv1505928	Remapped	Pass	GRCh37.p13	PATCHES	Second Pass	NW_004775431.1	Chr8\|NW_00 4775431.1	43,072	53,127
esv1505928	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000008.9	Chr8	48,377,484	48,388,781

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
essv3641514	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
essv3641514	Remapped	Pass	NC_000008.11:g.473 06914_47316969inv	GRCh38.p12	First Pass	NC_000008.11	Chr8	47,306,914	47,316,969
essv3641514	Remapped	Pass	NW_004775431.1:g.4 3072_53127inv	GRCh37.p13	Second Pass	NW_004775431.1	Chr8\|NW_00 4775431.1	43,072	53,127
essv3641514	Remapped	Perfect	NC_000008.10:g.482 14931_48226228inv	GRCh37.p13	First Pass	NC_000008.10	Chr8	48,214,931	48,226,228
essv3641514	Submitted genomic		NC_000008.9:g.4837 7484_48388781inv	NCBI36 (hg18)		NC_000008.9	Chr8	48,377,484	48,388,781

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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