A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv755905



Internal ID15703175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94920508..94974582hg38UCSC Ensembl
Innerchr10:96680265..96734339hg19UCSC Ensembl
Innerchr10:96670255..96724329hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3854075
hg1954075
hg1854075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551962
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)nssv755905
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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