A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791531



Internal ID19169292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:124761722..124965250hg38UCSC Ensembl
Innerchr8:125773964..125977492hg19UCSC Ensembl
Innerchr8:125843145..126046673hg18UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38203529
hg19203529
hg18203529
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891476
Supporting Variants
Samples
Known GenesLINC00964, MIR4662A, MIR4662B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=65
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791531
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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