A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785593



Internal ID18833299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:188284250..189430689hg38UCSC Ensembl
Innerchr4:189205404..190351843hg19UCSC Ensembl
Innerchr4:189442398..190588837hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg381146440
hg191146440
hg181146440
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894095
Supporting Variants
Samples
Known GenesLINC01060
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=316
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785593
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