A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798417



Internal ID18815356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28172111..28181904hg38UCSC Ensembl
Innerchr10:28461040..28470833hg19UCSC Ensembl
Innerchr10:28501046..28510839hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg389794
hg199794
hg189794
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891779
Supporting Variants
Samples
Known GenesMPP7
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798417
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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