A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036149



Internal ID19125368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3161307..3326824hg38UCSC Ensembl
Innerchr16:3211308..3376824hg19UCSC Ensembl
Innerchr16:3151309..3316825hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38165518
hg19165517
hg18165517
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3556961
Samples
Known GenesLINC00921, MEFV, OR1F1, OR1F2P, TIGD7, ZNF200, ZNF263, ZNF75A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036149
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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