A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065291



Internal ID18807822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:85023601..85049104hg38UCSC Ensembl
Innerchr16:85057207..85082710hg19UCSC Ensembl
Innerchr16:83614708..83640211hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3825504
hg1925504
hg1825504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3719113
Samples
Known GenesKIAA0513
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065291
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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