A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657192



Internal ID15047158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143133530..143184447hg38UCSC Ensembl
Innerchr7:142830623..142881540hg19UCSC Ensembl
Innerchr7:142540745..142591662hg18UCSC Ensembl
Innerchr7:142347460..142398377hg17UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3850918
hg1950918
hg1850918
hg1750918
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516782
Supporting Variants
Samples
Known GenesPIP, TAS2R39
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657192
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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