A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015389



Internal ID19104606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:34213047..34484641hg38UCSC Ensembl
Innerchr5:34213152..34484746hg19UCSC Ensembl
Innerchr5:34248909..34520503hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38271595
hg19271595
hg18271595
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5628n100
Supporting Variantsnssv3637058
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)nsv1015389
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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