A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1028954



Internal ID15882140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:36433680..36459973hg38UCSC Ensembl
Innerchr5:36433782..36460075hg19UCSC Ensembl
Innerchr5:36469539..36495832hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3826294
hg1926294
hg1826294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597817
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1028954
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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