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dbVar

Database of genomic structural variation

nsv4760380

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:25,303

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: 363 SVs from 65 studies. See in: genome view

Remapped(Score: Perfect):131,768,534-131,793,836

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4760380	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000002.12	Chr2	131,768,534	131,793,836
nsv4760380	Remapped	Pass	GRCh38.p12	ALT_REF_LOCI_1	Second Pass	NT_187528.1	Chr2\|NT_18 7528.1	75,406	97,829
nsv4760380	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000002.11	Chr2	132,526,107	132,551,409

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16284776	inversion	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16284776	Remapped	Pass	NT_187528.1:g.7540 6_97829inv	GRCh38.p12	Second Pass	NT_187528.1	Chr2\|NT_18 7528.1	75,406	97,829
nssv16284776	Remapped	Perfect	NC_000002.12:g.131 768534_131793836in v	GRCh38.p12	First Pass	NC_000002.12	Chr2	131,768,534	131,793,836
nssv16284776	Submitted genomic		NC_000002.11:g.132 526107_132551409in v	GRCh37 (hg19)		NC_000002.11	Chr2	132,526,107	132,551,409

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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