A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612295



Internal ID16399704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:130839022..130839898hg38UCSC Ensembl
Innerchr8:131851268..131852144hg19UCSC Ensembl
Innerchr8:131920450..131921326hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38877
hg19877
hg18877
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1121331
Samples
Known GenesADCY8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612295
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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