A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1021236



Internal ID16315192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:472511..473374hg38UCSC Ensembl
Innerchr5:472626..473489hg19UCSC Ensembl
Innerchr5:525626..526489hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38864
hg19864
hg18864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596678
Supporting Variants
Samples
Known GenesPP7080, SLC9A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1021236
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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