A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1124958



Internal ID15978144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:143147686..143256883hg38UCSC Ensembl
Innerchr8:144229103..144339053hg19UCSC Ensembl
Innerchr8:144300478..144410428hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38109198
hg19109951
hg18109951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612726
Supporting Variants
Samples
Known GenesGPIHBP1, LY6H, ZFP41
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1124958
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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