A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13683804



Internal ID21205661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:94950282..94950591hg38UCSC Ensembl
chr12:95344058..95344367hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2792918
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13683804
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.4375


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