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dbVar

Database of genomic structural variation

nsv5944629

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:284

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: 591 SVs from 52 studies. See in: genome view

Submitted genomic79,694,244-79,694,527

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5944629	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000018.10	Chr18	79,694,244	79,694,527
nsv5944629	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	77,454,244	77,454,527

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17394987	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17394987	Submitted genomic		NC_000018.10:g.796 94244_79694527del	GRCh38 (hg38)		NC_000018.10	Chr18	79,694,244	79,694,527
nssv17394987	Remapped	Perfect	NC_000018.9:g.7745 4244_77454527del	GRCh37.p13	First Pass	NC_000018.9	Chr18	77,454,244	77,454,527

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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