A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067305



Internal ID19156524
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 StatusM
Merged Variantsdgv3014n100
Supporting Variantsnssv3559552
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)nsv1067305
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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