A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039270



Internal ID19128489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94738127..94805859hg38UCSC Ensembl
Innerchr10:96497884..96565616hg19UCSC Ensembl
Innerchr10:96487874..96555606hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3867733
hg1967733
hg1867733
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv957n100
Supporting Variantsnssv3505767
Samples
Known GenesCYP2C19
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039270
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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