A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156101



Internal ID15528204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143070653..143184447hg38UCSC Ensembl
Innerchr7:142767750..142881540hg19UCSC Ensembl
Innerchr7:142477872..142591662hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38113795
hg19113791
hg18113791
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608657
Supporting Variants
SamplesHGDP00606
Known GenesPIP, TAS2R39
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156101
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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