A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv616006



Internal ID16403415
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 StatusM
Merged Variants
Supporting Variantsnssv1148360
Samples
Known GenesSAPCD2, UAP1L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv616006
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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