A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1140996



Internal ID15647496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105442981..105535902hg38UCSC Ensembl
Innerchr9:108205262..108298183hg19UCSC Ensembl
Innerchr9:107245083..107338004hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3892922
hg1992922
hg1892922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615115
Supporting Variants
Samples
Known GenesFSD1L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1140996
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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