A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064546



Internal ID18807077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:74834897..74955590hg38UCSC Ensembl
Innerchr16:74868795..74989488hg19UCSC Ensembl
Innerchr16:73426296..73546989hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38120694
hg19120694
hg18120694
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3019n100
Supporting Variantsnssv3559578
Samples
Known GenesWDR59
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064546
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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