A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891740



Internal ID18839450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3052854..3058244hg38UCSC Ensembl
Outerchr10:3052854..3058244hg38UCSC Ensembl
Innerchr10:3095046..3100436hg19UCSC Ensembl
Outerchr10:3095046..3100436hg19UCSC Ensembl
Innerchr10:3085046..3090436hg18UCSC Ensembl
Outerchr10:3085046..3090436hg18UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg385391
hg195391
hg185391
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796624
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891740
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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