A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610423



Internal ID16397832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:13617769..13669212hg38UCSC Ensembl
Innerchr8:13475278..13526721hg19UCSC Ensembl
Innerchr8:13519649..13571092hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3851444
hg1951444
hg1851444
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155987
SamplesHGDP00080
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610423
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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