A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv755906



Internal ID15703176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94960505..94984186hg38UCSC Ensembl
Innerchr10:96720262..96743943hg19UCSC Ensembl
Innerchr10:96710252..96733933hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3823682
hg1923682
hg1823682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551963
Supporting Variants
Samples
Known GenesCYP2C9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv755906
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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