A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3557987



Internal ID18509582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15966537..16196638hg38UCSC Ensembl
Innerchr16:16060394..16290495hg19UCSC Ensembl
Innerchr16:15967895..16197996hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38230102
hg19230102
hg18230102
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053451
Supporting Variants
Samples
Known GenesABCC1, ABCC6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3557987
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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