A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571548



Internal ID16012271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:16152307..16166485hg38UCSC Ensembl
Innerchr16:16246164..16260342hg19UCSC Ensembl
Innerchr16:16153665..16167843hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3814179
hg1914179
hg1814179
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4927n54
Supporting Variantsnssv852823
Samples
Known GenesABCC6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571548
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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