A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155232



Internal ID15856001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:132180333..132194503hg38UCSC Ensembl
Innerchr7:131865092..131879262hg19UCSC Ensembl
Innerchr7:131515632..131529802hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3814171
hg1914171
hg1814171
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608438
Supporting Variants
Samples1798860306_A
Known GenesPLXNA4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155232
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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