A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610677



Internal ID16051400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:17355620..17446698hg38UCSC Ensembl
Innerchr8:17213129..17304207hg19UCSC Ensembl
Innerchr8:17257500..17348578hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3891079
hg1991079
hg1891079
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156346
SamplesHGDP00905
Known GenesMTMR7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610677
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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