A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1026285



Internal ID16320241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:16179136..16180006hg38UCSC Ensembl
Innerchr5:16179245..16180115hg19UCSC Ensembl
Innerchr5:16232245..16233115hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38871
hg19871
hg18871
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597305
Supporting Variants
Samples
Known GenesMARCH11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1026285
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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