A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1096521



Internal ID15603021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143133530..143239150hg38UCSC Ensembl
Innerchr7:142830623..142936243hg19UCSC Ensembl
Innerchr7:142540745..142646365hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38105621
hg19105621
hg18105621
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608673
Supporting Variants
Samples
Known GenesPIP, TAS2R39, TAS2R40
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1096521
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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