A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571460



Internal ID16358869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12087845..12144745hg38UCSC Ensembl
Innerchr16:12181702..12238602hg19UCSC Ensembl
Innerchr16:12089203..12146103hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3856901
hg1956901
hg1856901
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852533
Samples
Known GenesSNX29
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571460
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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