A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796624



Internal ID18823508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3052854..3058244hg38UCSC Ensembl
Innerchr10:3095046..3100436hg19UCSC Ensembl
Innerchr10:3085046..3090436hg18UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg385391
hg195391
hg185391
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891740
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796624
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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