A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610576



Internal ID16397985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:16070177..16381359hg38UCSC Ensembl
Innerchr8:15927686..16238868hg19UCSC Ensembl
Innerchr8:15972057..16283239hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38311183
hg19311183
hg18311183
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1106954
Samples
Known GenesMSR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610576
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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