A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148356



Internal ID15654856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136977855..136981118hg38UCSC Ensembl
Innerchr9:139872307..139875570hg19UCSC Ensembl
Innerchr9:138992128..138995391hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg383264
hg193264
hg183264
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv616002
Supporting Variants
Samples
Known GenesPTGDS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148356
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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