A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv843333



Internal ID15790603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:55263404..55544506hg38UCSC Ensembl
Innerchr15:55555602..55836704hg19UCSC Ensembl
Innerchr15:53342894..53623996hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38281103
hg19281103
hg18281103
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569523
Supporting Variants
Samples
Known GenesC15orf65, CCPG1, DYX1C1, DYX1C1-CCPG1, MIR628, PIGB, RAB27A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv843333
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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