A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610471



Internal ID16397880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:14504729..14796607hg38UCSC Ensembl
Innerchr8:14362238..14654116hg19UCSC Ensembl
Innerchr8:14406609..14698487hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38291879
hg19291879
hg18291879
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156300
SamplesHGDP00631
Known GenesSGCZ
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610471
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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