A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852805



Internal ID15800075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15041412..15099845hg38UCSC Ensembl
Innerchr16:15135269..15193702hg19UCSC Ensembl
Innerchr16:15042770..15101203hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3858434
hg1958434
hg1858434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571529
Supporting Variants
Samples
Known GenesNTAN1, PDXDC1, RRN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852805
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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