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dbVar

Database of genomic structural variation

nsv5968213

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Almarri et al. 2020

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: 153 SVs from 30 studies. See in: genome view

Submitted genomic69,303,837-69,303,837

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5968213	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	69,303,837	69,303,837
nsv5968213	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	67,299,978	67,299,978

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17373738	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17373738	Submitted genomic		NC_000017.11:g.693 03837_69303838ins6 4	GRCh38 (hg38)		NC_000017.11	Chr17	69,303,837	69,303,837
nssv17373738	Remapped	Perfect	NC_000017.10:g.672 99978_67299979ins6 4	GRCh37.p13	First Pass	NC_000017.10	Chr17	67,299,978	67,299,978

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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