A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1028860



Internal ID15882046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:32100606..32169441hg38UCSC Ensembl
Innerchr5:32100712..32169547hg19UCSC Ensembl
Innerchr5:32136469..32205304hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3868836
hg1968836
hg1868836
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597768
Supporting Variants
Samples
Known GenesGOLPH3, PDZD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1028860
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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