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dbVar

Database of genomic structural variation

nsv4755756

Organism: Homo sapiens

Study:nstd199 (Quan et al. 2021)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:24,038

Publication(s):Quan et al. 2021

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: 318 SVs from 70 studies. See in: genome view

Remapped(Score: Perfect):1,915,730-1,939,767

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4755756	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	1,915,730	1,939,767
nsv4755756	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000011.9	Chr11	1,936,960	1,960,997

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16263587	inversion	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16263587	Remapped	Perfect	NC_000011.10:g.191 5730_1939767inv	GRCh38.p12	First Pass	NC_000011.10	Chr11	1,915,730	1,939,767
nssv16263587	Submitted genomic		NC_000011.9:g.1936 960_1960997inv	GRCh37 (hg19)		NC_000011.9	Chr11	1,936,960	1,960,997

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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