A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559657



Internal ID18511252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:76969529..77433389hg38UCSC Ensembl
Innerchr16:77003426..77467286hg19UCSC Ensembl
Innerchr16:75560927..76024787hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38463861
hg19463861
hg18463861
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055234
Supporting Variants
Samples
Known GenesADAMTS18, MON1B, SYCE1L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559657
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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