A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615213



Internal ID16055936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113143570..113174623hg38UCSC Ensembl
Innerchr9:115905850..115936903hg19UCSC Ensembl
Innerchr9:114945671..114976724hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3831054
hg1931054
hg1831054
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176139
SamplesHGDP01171
Known GenesFKBP15, SLC31A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615213
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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