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dbVar

Database of genomic structural variation

esv1290018

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:2,826

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: 304 SVs from 35 studies. See in: genome view

Remapped(Score: Perfect):12,144,390-12,147,215

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv1290018	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000018.10	Chr18	12,144,390	12,147,215
esv1290018	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	12,144,389	12,147,214
esv1290018	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000018.8	Chr18	12,134,389	12,137,214

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
essv4357480	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
essv4357480	Remapped	Perfect	NC_000018.10:g.121 44390_12147215inv	GRCh38.p12	First Pass	NC_000018.10	Chr18	12,144,390	12,147,215
essv4357480	Remapped	Perfect	NC_000018.9:g.1214 4389_12147214inv	GRCh37.p13	First Pass	NC_000018.9	Chr18	12,144,389	12,147,214
essv4357480	Submitted genomic		NC_000018.8:g.1213 4389_12137214inv	NCBI36 (hg18)		NC_000018.8	Chr18	12,134,389	12,137,214

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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