A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559438



Internal ID18857719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:65332087..65450341hg38UCSC Ensembl
Innerchr16:65365990..65484244hg19UCSC Ensembl
Innerchr16:63923491..64041745hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38118255
hg19118255
hg18118255
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057264
Supporting Variants
Samples
Known GenesLINC00922
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559438
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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