A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032784



Internal ID19122006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:23791656..24195698hg38UCSC Ensembl
Innerchr5:23791765..24195807hg19UCSC Ensembl
Innerchr5:23827522..24231564hg18UCSC Ensembl
Cytoband5p14.2
Allele length
AssemblyAllele length
hg38404043
hg19404043
hg18404043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635945
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)nsv1032784
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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