A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612771



Internal ID16400180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:143476995..143529559hg38UCSC Ensembl
Innerchr8:144559165..144611729hg19UCSC Ensembl
Innerchr8:144630308..144682872hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3852565
hg1952565
hg1852565
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156659
SamplesHGDP00864
Known GenesZC3H3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612771
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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