A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3511751



Internal ID18463346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94645539..94755237hg38UCSC Ensembl
Innerchr10:96405296..96514994hg19UCSC Ensembl
Innerchr10:96395286..96504984hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38109699
hg19109699
hg18109699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040106
Supporting Variants
Samples
Known GenesCYP2C18
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3511751
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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