A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040106



Internal ID18782637
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 StatusM
Merged Variantsdgv955n100
Supporting Variantsnssv3511751
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)nsv1040106
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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