A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056617



Internal ID18799148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35309340..36048843hg38UCSC Ensembl
Innerchr16:34543711..35283214hg19UCSC Ensembl
Innerchr16:34401212..35140715hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38739504
hg19739504
hg18739504
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559085
Samples
Known GenesFLJ26245, LOC100130700, 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)nsv1056617
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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