A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786178



Internal ID19162119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:95105048..95153599hg38UCSC Ensembl
Innerchr10:96864805..96913356hg19UCSC Ensembl
Innerchr10:96854795..96903346hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3848552
hg1948552
hg1848552
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891887
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786178
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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