A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13703287



Internal ID21225100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122705696..122705957hg38UCSC Ensembl
chr7:122345750..122346011hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2813963
Supporting Variants
Samples
Known GenesCADPS2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13703287
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.725806


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