A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038196



Internal ID18780727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3917410..4153984hg38UCSC Ensembl
Innerchr16:3967411..4203985hg19UCSC Ensembl
Innerchr16:3907412..4143986hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38236575
hg19236575
hg18236575
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3556968
Samples
Known GenesADCY9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038196
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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