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dbVar

Database of genomic structural variation

nsv5959367

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: 130 SVs from 22 studies. See in: genome view

Submitted genomic44,270,798-44,270,798

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5959367	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	44,270,798	44,270,798
nsv5959367	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	44,736,470	44,736,470

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17388830	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17388830	Submitted genomic		NC_000001.11:g.442 70798_44270799ins5 94	GRCh38 (hg38)		NC_000001.11	Chr1	44,270,798	44,270,798
nssv17388830	Remapped	Perfect	NC_000001.10:g.447 36470_44736471ins5 94	GRCh37.p13	First Pass	NC_000001.10	Chr1	44,736,470	44,736,470

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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