A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025678



Internal ID19114896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:112030169..112081501hg38UCSC Ensembl
Innerchr5:111365866..111417198hg19UCSC Ensembl
Innerchr5:111393765..111445097hg18UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3851333
hg1951333
hg1851333
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3647051
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)nsv1025678
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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