A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3662125



Internal ID18613720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:122726490..123352883hg38UCSC Ensembl
Innerchr7:122366544..122992937hg19UCSC Ensembl
Innerchr7:122153780..122780173hg18UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38626394
hg19626394
hg18626394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033520
Supporting Variants
Samples
Known GenesCADPS2, SLC13A1, TAS2R16
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3662125
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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