A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615847



Internal ID16403256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135254963..135400692hg38UCSC Ensembl
Innerchr9:138146809..138292538hg19UCSC Ensembl
Innerchr9:137286630..137432359hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38145730
hg19145730
hg18145730
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12979n54
Supporting Variantsnssv1146789
Samples
Known GenesC9orf62
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615847
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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