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dbVar

Database of genomic structural variation

nsv5975894

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: 84 SVs from 17 studies. See in: genome view

Submitted genomic47,540,540-47,540,540

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5975894	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000014.9	Chr14	47,540,540	47,540,540
nsv5975894	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	48,009,743	48,009,743

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17381354	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17381354	Submitted genomic		NC_000014.9:g.4754 0540_47540541ins50	GRCh38 (hg38)		NC_000014.9	Chr14	47,540,540	47,540,540
nssv17381354	Remapped	Perfect	NC_000014.8:g.4800 9743_48009744ins50	GRCh37.p13	First Pass	NC_000014.8	Chr14	48,009,743	48,009,743

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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