A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551961



Internal ID15992684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94740349..94788375hg38UCSC Ensembl
Innerchr10:96500106..96548132hg19UCSC Ensembl
Innerchr10:96490096..96538122hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3848027
hg1948027
hg1848027
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1356n54
Supporting Variantsnssv755903, nssv755902, nssv755904
Samples
Known GenesCYP2C19
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551961
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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