A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1125795



Internal ID15632295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:144390576..144397883hg38UCSC Ensembl
Innerchr8:145615776..145623098hg19UCSC Ensembl
Innerchr8:145586584..145593906hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg387308
hg197323
hg187323
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612934
Supporting Variants
Samples
Known GenesADCK5, CPSF1, MIR939
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1125795
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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