A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571551



Internal ID16012274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:16153614..16161580hg38UCSC Ensembl
Innerchr16:16247471..16255437hg19UCSC Ensembl
Innerchr16:16154972..16162938hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg387967
hg197967
hg187967
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852830
Samples
Known GenesABCC6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571551
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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