A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034539



Internal ID18777073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:12417058..12711264hg38UCSC Ensembl
Innerchr5:12417170..12711376hg19UCSC Ensembl
Innerchr5:12470170..12764376hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38294207
hg19294207
hg18294207
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3638207
Samples
Known GenesCT49
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034539
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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