A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779645



Internal ID19167252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:161852857..162204891hg38UCSC Ensembl
Innerchr3:161570645..161922679hg19UCSC Ensembl
Innerchr3:163053339..163405373hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38352035
hg19352035
hg18352035
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893793
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=88
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779645
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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