A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15179625



Internal ID21318421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33563398..33563447hg38UCSC Ensembl
chr21:34935704..34935753hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3929192
Supporting Variants
SamplesHG002
Known GenesSON
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15179625
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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