A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv616001



Internal ID16403410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136977855..136980285hg38UCSC Ensembl
Innerchr9:139872307..139874737hg19UCSC Ensembl
Innerchr9:138992128..138994558hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg382431
hg192431
hg182431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv13008n54
Supporting Variantsnssv1148355
Samples
Known GenesPTGDS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv616001
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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