A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019851



Internal ID19109069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:676322..779733hg38UCSC Ensembl
Innerchr5:676437..779848hg19UCSC Ensembl
Innerchr5:729437..832848hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38103412
hg19103412
hg18103412
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5523n100
Supporting Variantsnssv3633265, nssv3745329, nssv3633264
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)nsv1019851
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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