A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610267



Internal ID16050990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:10411226..10669232hg38UCSC Ensembl
Innerchr8:10268736..10526742hg19UCSC Ensembl
Innerchr8:10306146..10564152hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38258007
hg19258007
hg18258007
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1106252
Samples
Known GenesMIR4286, MSRA, PRSS55, RP1L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610267
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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