A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611759



Internal ID16399168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:95208894..95235607hg38UCSC Ensembl
Innerchr8:96221122..96247835hg19UCSC Ensembl
Innerchr8:96290298..96317011hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3826714
hg1926714
hg1826714
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156633
SamplesHGDP00757
Known GenesC8orf69
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611759
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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