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dbVar

Database of genomic structural variation

nsv5948307

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: 148 SVs from 19 studies. See in: genome view

Submitted genomic200,657,412-200,657,412

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5948307	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	200,657,412	200,657,412
nsv5948307	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	201,522,135	201,522,135

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17407663	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17407663	Submitted genomic		NC_000002.12:g.200 657412_200657413in s59	GRCh38 (hg38)		NC_000002.12	Chr2	200,657,412	200,657,412
nssv17407663	Remapped	Perfect	NC_000002.11:g.201 522135_201522136in s59	GRCh37.p13	First Pass	NC_000002.11	Chr2	201,522,135	201,522,135

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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