A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610586



Internal ID16397995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:16092262..16158503hg38UCSC Ensembl
Innerchr8:15949771..16016012hg19UCSC Ensembl
Innerchr8:15994142..16060383hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3866242
hg1966242
hg1866242
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12022n54
Supporting Variantsnssv1156334
Samples1780862306_A
Known GenesMSR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610586
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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