A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026664



Internal ID19115882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:2626426..2648402hg38UCSC Ensembl
Innerchr5:2626540..2648516hg19UCSC Ensembl
Innerchr5:2679540..2701516hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3821977
hg1921977
hg1821977
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5553n100
Supporting Variantsnssv3638518
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)nsv1026664
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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