A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3556149



Internal ID18854430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35232188..35496900hg38UCSC Ensembl
Innerchr16:34466559..34731271hg19UCSC Ensembl
Innerchr16:34324060..34588772hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38264713
hg19264713
hg18264713
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056720
Supporting Variants
Samples
Known GenesLOC146481, LOC283914
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3556149
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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