A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148360



Internal ID16001546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:137057859..137083633hg38UCSC Ensembl
Innerchr9:139952311..139978085hg19UCSC Ensembl
Innerchr9:139072132..139097906hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3825775
hg1925775
hg1825775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv616006
Supporting Variants
Samples
Known GenesSAPCD2, UAP1L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148360
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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