A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036374



Internal ID18778905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8970392..9111577hg38UCSC Ensembl
Innerchr16:9064249..9205434hg19UCSC Ensembl
Innerchr16:8971750..9112935hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38141186
hg19141186
hg18141186
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2726n100
Supporting Variantsnssv3557114
Samples
Known GenesC16orf72
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036374
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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