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dbVar

Database of genomic structural variation

nsv5964042

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

Submitted genomic35,501,993-35,501,993

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5964042	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	35,501,993	35,501,993
nsv5964042	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	35,520,110	35,520,110

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17469618	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17469618	Submitted genomic		NC_000023.11:g.355 01993_35501994ins4 68	GRCh38 (hg38)		NC_000023.11	ChrX	35,501,993	35,501,993
nssv17469618	Remapped	Perfect	NC_000023.10:g.355 20110_35520111ins4 68	GRCh37.p13	First Pass	NC_000023.10	ChrX	35,520,110	35,520,110

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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