A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045575



Internal ID18788106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133438600..133586746hg38UCSC Ensembl
Innerchr10:135252104..135400250hg19UCSC Ensembl
Innerchr10:135102094..135250240hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38148147
hg19148147
hg18148147
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1004n100
Supporting Variantsnssv3515351
Samples
Known GenesCYP2E1, SCART1, SPRNP1, SYCE1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045575
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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