A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094166



Internal ID20661206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132391982..132422290hg38UCSC Ensembl
chr3:132110826..132141134hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3830309
hg1930309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6366394
Supporting Variants
Samples
Known GenesDNAJC13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094166
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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