A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784623



Internal ID19177597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:188223645..188995666hg38UCSC Ensembl
Innerchr4:189144799..189916820hg19UCSC Ensembl
Innerchr4:189381793..190153814hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38772022
hg19772022
hg18772022
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894094
Supporting Variants
Samples
Known GenesLINC01060
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=221
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784623
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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