A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891795



Internal ID18839505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42298677..42690427hg38UCSC Ensembl
Outerchr10:42298677..42690427hg38UCSC Ensembl
Innerchr10:42794125..43185875hg19UCSC Ensembl
Outerchr10:42794125..43185875hg19UCSC Ensembl
Innerchr10:42114131..42505881hg18UCSC Ensembl
Outerchr10:42114131..42505881hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38391751
hg19391751
hg18391751
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787947
Samples
Known GenesCCNYL2, LINC00839, LOC441666, ZNF33B, ZNF37BP
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891795
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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