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dbVar

Database of genomic structural variation

nsv4755375

Organism: Homo sapiens

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

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

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: 83 SVs from 20 studies. See in: genome view

Remapped(Score: Perfect):39,906,059-39,906,059

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4755375	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	39,906,059	39,906,059
nsv4755375	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000006.11	Chr6	39,873,835	39,873,835

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16260929	insertion	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16260929	Remapped	Perfect	NC_000006.12:g.399 06059_39906060ins9 0	GRCh38.p12	First Pass	NC_000006.12	Chr6	39,906,059	39,906,059
nssv16260929	Submitted genomic		NC_000006.11:g.398 73835_39873836ins9 0	GRCh37 (hg19)		NC_000006.11	Chr6	39,873,835	39,873,835

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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