A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559240



Internal ID18510835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:46429858..46621604hg38UCSC Ensembl
Innerchr16:46463770..46655516hg19UCSC Ensembl
Innerchr16:45021271..45213017hg18UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg38191747
hg19191747
hg18191747
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056162
Supporting Variants
Samples
Known GenesANKRD26P1, SHCBP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559240
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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