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dbVar

Database of genomic structural variation

nsv5645027

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Ebert et al. 2021

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: 167 SVs from 36 studies. See in: genome view

Submitted genomic24,082,520-24,082,520

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5645027	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	24,082,520	24,082,520
nsv5645027	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	24,265,322	24,265,322

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17104036	insertion	SAMN00006579	Sequencing	Sequence alignment	23,265

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17104036	Submitted genomic		NC_000019.10:g.240 82520_24082521ins2 547	GRCh38 (hg38)		NC_000019.10	Chr19	24,082,520	24,082,520
nssv17104036	Remapped	Perfect	NC_000019.9:g.2426 5322_24265323ins25 47	GRCh37.p13	First Pass	NC_000019.9	Chr19	24,265,322	24,265,322

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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