A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148898



Internal ID15527232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1965120..2020567hg38UCSC Ensembl
Innerchr16:2015121..2070568hg19UCSC Ensembl
Innerchr16:1955122..2010569hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3855448
hg1955448
hg1855448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571183
Supporting Variants
SamplesHGDP00433
Known GenesGFER, NOXO1, NPW, RNF151, SNHG9, SNORA78, SYNGR3, TBL3, ZNF598
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148898
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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