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dbVar

Database of genomic structural variation

nsv5957400

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: 110 SVs from 26 studies. See in: genome view

Submitted genomic148,213,590-148,213,590

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5957400	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	148,213,590	148,213,590
nsv5957400	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	148,534,726	148,534,726

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17422775	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17422775	Submitted genomic		NC_000006.12:g.148 213590_148213591in s317	GRCh38 (hg38)		NC_000006.12	Chr6	148,213,590	148,213,590
nssv17422775	Remapped	Perfect	NC_000006.11:g.148 534726_148534727in s317	GRCh37.p13	First Pass	NC_000006.11	Chr6	148,534,726	148,534,726

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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