A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024747



Internal ID19113964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:113257013..113343676hg38UCSC Ensembl
Innerchr5:112592710..112679373hg19UCSC Ensembl
Innerchr5:112620609..112707272hg18UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg3886664
hg1986664
hg1886664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3647060
Samples
Known GenesMCC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024747
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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