A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852799



Internal ID15800069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14961008..15040518hg38UCSC Ensembl
Innerchr16:15054865..15134375hg19UCSC Ensembl
Innerchr16:14962366..15041876hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3879511
hg1979511
hg1879511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571524
Supporting Variants
Samples
Known GenesMIR1972-1, MIR1972-2, NTAN1, PDXDC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852799
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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