A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1124933



Internal ID15631433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:142564638..142670446hg38UCSC Ensembl
Innerchr8:143645999..143751864hg19UCSC Ensembl
Innerchr8:143643001..143748866hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38105809
hg19105866
hg18105866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612709
Supporting Variants
Samples
Known GenesARC, JRK, PSCA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1124933
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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