A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718869



Internal ID18670464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8678512..8730293hg38UCSC Ensembl
Innerchr16:8772369..8824150hg19UCSC Ensembl
Innerchr16:8679870..8731651hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3851782
hg1951782
hg1851782
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035233
Supporting Variants
Samples
Known GenesABAT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3718869
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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