A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571546



Internal ID16012269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15979799..16012108hg38UCSC Ensembl
Innerchr16:16073656..16105965hg19UCSC Ensembl
Innerchr16:15981157..16013466hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3832310
hg1932310
hg1832310
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852822
Samples
Known GenesABCC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571546
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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