A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3558289



Internal ID18856570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35232188..35526596hg38UCSC Ensembl
Innerchr16:34466559..34760967hg19UCSC Ensembl
Innerchr16:34324060..34618468hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38294409
hg19294409
hg18294409
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059628
Supporting Variants
Samples
Known GenesLOC100130700, LOC146481, LOC283914
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3558289
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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