A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989716



Internal ID20556756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31819445..31819805hg38UCSC Ensembl
chr11:31840992..31841352hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443502
Supporting Variants
Samples
Known GenesDKFZp686K1684
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989716
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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