A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3947611



Internal ID21367680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122419595..122419921hg38UCSC Ensembl
chr3:122138442..122138768hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15179858
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3947611
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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