A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559552



Internal ID18857833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70820478..70988626hg38UCSC Ensembl
Innerchr16:70854381..71022529hg19UCSC Ensembl
Innerchr16:69411882..69580030hg18UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg38168149
hg19168149
hg18168149
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1067305
Supporting Variants
Samples
Known GenesHYDIN, HYDIN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559552
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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