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dbVar

Database of genomic structural variation

nsv5957630

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: 159 SVs from 33 studies. See in: genome view

Submitted genomic123,108,260-123,108,260

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5957630	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	123,108,260	123,108,260
nsv5957630	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	124,029,415	124,029,415

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17412016	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17412016	Submitted genomic		NC_000004.12:g.123 108260_123108261in s50	GRCh38 (hg38)		NC_000004.12	Chr4	123,108,260	123,108,260
nssv17412016	Remapped	Perfect	NC_000004.11:g.124 029415_124029416in s50	GRCh37.p13	First Pass	NC_000004.11	Chr4	124,029,415	124,029,415

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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