A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571214



Internal ID16358623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:2607623..2649609hg38UCSC Ensembl
Innerchr16:2657624..2699610hg19UCSC Ensembl
Innerchr16:2597625..2639611hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3841987
hg1941987
hg1841987
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852107
Samples
Known GenesFLJ42627, LOC652276
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571214
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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