A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1125948



Internal ID15979134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:320856..322405hg38UCSC Ensembl
Innerchr9:320856..322405hg19UCSC Ensembl
Innerchr9:310856..312405hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg381550
hg191550
hg181550
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613009
Supporting Variants
Samples
Known GenesDOCK8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1125948
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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