A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611819



Internal ID16399228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:101834974..101917232hg38UCSC Ensembl
Innerchr8:102847202..102929460hg19UCSC Ensembl
Innerchr8:102916378..102998636hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3882259
hg1982259
hg1882259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156143
SamplesHGDP00625
Known GenesNCALD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611819
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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