A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064977



Internal ID18807508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83476129..83856075hg38UCSC Ensembl
Innerchr16:83509734..83889680hg19UCSC Ensembl
Innerchr16:82067235..82447181hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38379947
hg19379947
hg18379947
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559933
Samples
Known GenesCDH13, HSBP1, MIR3182
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064977
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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