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dbVar

Database of genomic structural variation

nsv5943335

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:312

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: 182 SVs from 21 studies. See in: genome view

Submitted genomic24,030,837-24,031,148

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5943335	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000018.10	Chr18	24,030,837	24,031,148
nsv5943335	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	21,610,801	21,611,112

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17379763	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17379763	Submitted genomic		NC_000018.10:g.240 30837_24031148del	GRCh38 (hg38)		NC_000018.10	Chr18	24,030,837	24,031,148
nssv17379763	Remapped	Perfect	NC_000018.9:g.2161 0801_21611112del	GRCh37.p13	First Pass	NC_000018.9	Chr18	21,610,801	21,611,112

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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