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dbVar

Database of genomic structural variation

nsv3949853

Organism: Homo sapiens

Study:nstd167 (Wenger et al. 2019)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

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

Publication(s):Wenger et al. 2019

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: 26 SVs from 7 studies. See in: genome view

Remapped(Score: Perfect):59,209,899-59,209,899

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv3949853	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	59,209,899	59,209,899
nsv3949853	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000011.9	Chr11	58,977,372	58,977,372

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
nssv15190886	insertion	SAMN03283347	Sequencing	de novo and local sequence assembly	Heterozygous	30,634

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv15190886	Remapped	Perfect	NC_000011.10:g.592 09899_59209900ins8 4	GRCh38.p12	First Pass	NC_000011.10	Chr11	59,209,899	59,209,899
nssv15190886	Submitted genomic		NC_000011.9:g.5897 7372_58977373ins84	GRCh37 (hg19)		NC_000011.9	Chr11	58,977,372	58,977,372

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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