A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3638207



Internal ID18589802
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 StatusS
Merged Variantsnsv1034539
Supporting Variants
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)nssv3638207
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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