A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996653



Internal ID20563693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:100256242..100260404hg38UCSC Ensembl
chr12:100650020..100654182hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg384163
hg194163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6465088
Supporting Variants
Samples
Known GenesDEPDC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996653
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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