A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559964



Internal ID18511559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:85068826..85211361hg38UCSC Ensembl
Innerchr16:85102432..85244967hg19UCSC Ensembl
Innerchr16:83659933..83802468hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38142536
hg19142536
hg18142536
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058234
Supporting Variants
Samples
Known GenesFAM92B, KIAA0513, LOC400548
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559964
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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