A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612576



Internal ID16399985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:141323326..141378155hg38UCSC Ensembl
Innerchr8:142333425..142388255hg19UCSC Ensembl
Innerchr8:142402607..142457437hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3854830
hg1954831
hg1854831
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156891
SamplesHGDP00713
Known GenesGPR20, LOC731779
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612576
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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