A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989613



Internal ID20556653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31173800..31296425hg38UCSC Ensembl
chr11:31195347..31317972hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38122626
hg19122626
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449939
Supporting Variants
Samples
Known GenesDCDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989613
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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