A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610460



Internal ID16051183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:14037682..14115956hg38UCSC Ensembl
Innerchr8:13895191..13973465hg19UCSC Ensembl
Innerchr8:13939562..14017836hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3878275
hg1978275
hg1878275
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156295
SamplesHGDP01270
Known GenesSGCZ
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610460
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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