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dbVar

Database of genomic structural variation

esv1617544

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:21,495

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: 322 SVs from 69 studies. See in: genome view

Remapped(Score: Perfect):1,894,042-1,915,536

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv1617544	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	1,894,042	1,915,536
esv1617544	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	1,915,272	1,936,766
esv1617544	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000011.8	Chr11	1,871,848	1,893,342

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
essv3939709	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
essv3939709	Remapped	Perfect	NC_000011.10:g.189 4042_1915536inv	GRCh38.p12	First Pass	NC_000011.10	Chr11	1,894,042	1,915,536
essv3939709	Remapped	Perfect	NC_000011.9:g.1915 272_1936766inv	GRCh37.p13	First Pass	NC_000011.9	Chr11	1,915,272	1,936,766
essv3939709	Submitted genomic		NC_000011.8:g.1871 848_1893342inv	NCBI36 (hg18)		NC_000011.8	Chr11	1,871,848	1,893,342

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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