A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611563



Internal ID16398972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:75562484..75607599hg38UCSC Ensembl
Innerchr8:76474719..76519834hg19UCSC Ensembl
Innerchr8:76637274..76682389hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3845116
hg1945116
hg1845116
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156371
Samples1782681086_A
Known GenesHNF4G
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611563
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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