A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063531



Internal ID18806062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:25051972..25124743hg38UCSC Ensembl
Innerchr16:25063293..25136064hg19UCSC Ensembl
Innerchr16:24970794..25043565hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3872772
hg1972772
hg1872772
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2827n100
Supporting Variantsnssv3549130
Samples
Known GenesLCMT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063531
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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