A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv755900



Internal ID15703170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94739953..94797579hg38UCSC Ensembl
Innerchr10:96499710..96557336hg19UCSC Ensembl
Innerchr10:96489700..96547326hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3857627
hg1957627
hg1857627
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551959
Supporting Variants
Samples
Known GenesCYP2C19
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv755900
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer