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dbVar

Database of genomic structural variation

nsv499786

Organism: Homo sapiens

Study:nstd47 (Kidd et al. 2010b)
Variant Type:inversion
Method Type:Sequencing
Submitted on:NCBI36 (hg18)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:14,726

Publication(s):Kidd et al. 2010

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: 578 SVs from 81 studies. See in: genome view

Remapped(Score: Perfect):49,714,741-49,729,466

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv499786	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	49,714,741	49,729,466
nsv499786	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	49,736,293	49,751,018
nsv499786	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000011.8	Chr11	49,692,869	49,707,594

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv585496	inversion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv585496	Remapped	Perfect	NC_000011.10:g.497 14741_49729466inv	GRCh38.p12	First Pass	NC_000011.10	Chr11	49,714,741	49,729,466
nssv585496	Remapped	Perfect	NC_000011.9:g.4973 6293_49751018inv	GRCh37.p13	First Pass	NC_000011.9	Chr11	49,736,293	49,751,018
nssv585496	Submitted genomic		NC_000011.8:g.4969 2869_49707594inv	NCBI36 (hg18)		NC_000011.8	Chr11	49,692,869	49,707,594

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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