A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065714



Internal ID18808245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:77251762..77351621hg38UCSC Ensembl
Innerchr16:77285659..77385518hg19UCSC Ensembl
Innerchr16:75843160..75943019hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3899860
hg1999860
hg1899860
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559665
Samples
Known GenesADAMTS18
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065714
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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