A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1145407



Internal ID15998593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133256050..133256963hg38UCSC Ensembl
Innerchr9:136131437..136132350hg19UCSC Ensembl
Innerchr9:135121258..135122171hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38914
hg19914
hg18914
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615620
Supporting Variants
Samples
Known GenesABO
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1145407
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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