A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016601



Internal ID19105820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17601432..17721478hg38UCSC Ensembl
Innerchr5:17601541..17721587hg19UCSC Ensembl
Innerchr5:17644644..17757308hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38120047
hg19120047
hg18112665
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5588n100
Supporting Variantsnssv3635826, nssv3745820, nssv3635824, nssv3635825
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)nsv1016601
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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