A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610589



Internal ID16397998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:16092262..16171585hg38UCSC Ensembl
Innerchr8:15949771..16029094hg19UCSC Ensembl
Innerchr8:15994142..16073465hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3879324
hg1979324
hg1879324
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12022n54
Supporting Variantsnssv1156339, nssv1106983, nssv1106982, nssv1106980, nssv1106981, nssv1156338, nssv1156337
SamplesHGDP01402, NINDS_206, HGDP00886
Known GenesMSR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610589
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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