A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612709



Internal ID16053432
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 StatusM
Merged Variants
Supporting Variantsnssv1124933
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)nsv612709
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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