A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156445



Internal ID15879668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:18920359..18960395hg38UCSC Ensembl
Innerchr9:18920357..18960393hg19UCSC Ensembl
Innerchr9:18910357..18950393hg18UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3840037
hg1940037
hg1840037
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613727
Supporting Variants
SamplesHGDP01414
Known GenesFAM154A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156445
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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