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dbVar

Database of genomic structural variation

nsv5953558

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: 267 SVs from 47 studies. See in: genome view

Submitted genomic101,739,938-101,739,938

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5953558	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	101,739,938	101,739,938
nsv5953558	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	101,075,642	101,075,642

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17417379	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17417379	Submitted genomic		NC_000005.10:g.101 739938_101739939in s62	GRCh38 (hg38)		NC_000005.10	Chr5	101,739,938	101,739,938
nssv17417379	Remapped	Perfect	NC_000005.9:g.1010 75642_101075643ins 62	GRCh37.p13	First Pass	NC_000005.9	Chr5	101,075,642	101,075,642

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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