A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029125



Internal ID19118344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:685389..779733hg38UCSC Ensembl
Innerchr5:685504..779848hg19UCSC Ensembl
Innerchr5:738504..832848hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3894345
hg1994345
hg1894345
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5523n100
Supporting Variantsnssv3633295
Samples
Known GenesTPPP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029125
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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