A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520261



Internal ID15100868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143095565..143208912hg38UCSC Ensembl
Innerchr7:142792658..142906005hg19UCSC Ensembl
Innerchr7:142502780..142616127hg18UCSC Ensembl
Innerchr7:142309495..142422842hg17UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38113348
hg19113348
hg18113348
hg17113348
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv432n21
Supporting Variantsnssv697313
Samples
Known GenesPIP, TAS2R39
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520261
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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