A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148900



Internal ID15528348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:2004154..2037561hg38UCSC Ensembl
Innerchr16:2054155..2087562hg19UCSC Ensembl
Innerchr16:1994156..2027563hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3833408
hg1933408
hg1833408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571189
Supporting Variants
SamplesHGDP00626
Known GenesNPW, SLC9A3R2, ZNF598
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148900
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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