A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033520



Internal ID18776053
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 StatusM
Merged Variants
Supporting Variantsnssv3662125
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)nsv1033520
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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