A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612711



Internal ID16400120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:142574660..142612823hg38UCSC Ensembl
Innerchr8:143656021..143694184hg19UCSC Ensembl
Innerchr8:143653023..143691186hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3838164
hg1938164
hg1838164
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12397n54
Supporting Variantsnssv1156655
SamplesHGDP00619
Known GenesARC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612711
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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