A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799536



Internal ID19180563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:102640552..102727789hg38UCSC Ensembl
Innerchr4:103561709..103648946hg19UCSC Ensembl
Innerchr4:103780757..103867990hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3887238
hg1987238
hg1887234
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893999
Supporting Variants
Samples
Known GenesMANBA
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=20
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799536
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer