A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797242



Internal ID19170192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:56323877..56361440hg38UCSC Ensembl
Innerchr10:58083638..58121201hg19UCSC Ensembl
Innerchr10:57753644..57791207hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3837564
hg1937564
hg1837564
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891822
Supporting Variants
Samples
Known GenesZWINT
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797242
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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