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dbVar

Database of genomic structural variation

nsv5869468

Organism: Homo sapiens

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

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:303

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: 474 SVs from 44 studies. See in: genome view

Submitted genomic105,947,164-105,947,466

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5869468	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	105,947,164	105,947,466
nsv5869468	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	105,191,156	105,191,458

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17444981	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17444981	Submitted genomic		NC_000023.11:g.105 947164_105947466de l	GRCh38 (hg38)		NC_000023.11	ChrX	105,947,164	105,947,466
nssv17444981	Remapped	Perfect	NC_000023.10:g.105 191156_105191458de l	GRCh37.p13	First Pass	NC_000023.10	ChrX	105,191,156	105,191,458

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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