A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv616000



Internal ID16403409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136977693..136980181hg38UCSC Ensembl
Innerchr9:139872145..139874633hg19UCSC Ensembl
Innerchr9:138991966..138994454hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg382489
hg192489
hg182489
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv13008n54
Supporting Variantsnssv1148353, nssv1148354
Samples
Known GenesPTGDS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv616000
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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