A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049341



Internal ID18791872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94657052..94711479hg38UCSC Ensembl
Innerchr10:96416809..96471236hg19UCSC Ensembl
Innerchr10:96406799..96461226hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3854428
hg1954428
hg1854428
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv956n100
Supporting Variantsnssv3515871
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)nsv1049341
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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