A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032133



Internal ID19121355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:3687392..3806644hg38UCSC Ensembl
Innerchr5:3687506..3806758hg19UCSC Ensembl
Innerchr5:3740506..3859758hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38119253
hg19119253
hg18119253
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3746159
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032133
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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