A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25793074



Internal ID18827953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42097572..42452179hg38UCSC Ensembl
Innerchr10:42503182..42947627hg19UCSC Ensembl
Innerchr10:41823188..42267633hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg38354608
hg19444446
hg18444446
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891790
Supporting Variants
Samples
Known GenesCCNYL2, LOC441666
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
CommentsNumber of probes=25
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25793074
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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