A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615994



Internal ID16056717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136975930..136979942hg38UCSC Ensembl
Innerchr9:139870382..139874394hg19UCSC Ensembl
Innerchr9:138990203..138994215hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg384013
hg194013
hg184013
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148346
Samples
Known GenesPTGDS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615994
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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