A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893676



Internal ID19184496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:24984204..26577498hg38UCSC Ensembl
Outerchr3:24984204..26577498hg38UCSC Ensembl
Innerchr3:25025695..26618989hg19UCSC Ensembl
Outerchr3:25025695..26618989hg19UCSC Ensembl
Innerchr3:25000699..26593993hg18UCSC Ensembl
Outerchr3:25000699..26593993hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg381593295
hg191593295
hg181593295
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780520
Samples
Known GenesLINC00692, MIR4442, NGLY1, OXSM, RARB, TOP2B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893676
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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