A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3505767



Internal ID18804048
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 StatusS
Merged Variantsnsv1039270
Supporting Variants
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)nssv3505767
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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