A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611564



Internal ID16398973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:75564435..75566533hg38UCSC Ensembl
Innerchr8:76476670..76478768hg19UCSC Ensembl
Innerchr8:76639225..76641323hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg382099
hg192099
hg182099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1117005
Samples
Known GenesHNF4G
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611564
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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