A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25801358



Internal ID19160676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:177047424..177225465hg38UCSC Ensembl
Innerchr4:177968578..178146619hg19UCSC Ensembl
Innerchr4:178205572..178383613hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38178042
hg19178042
hg18178042
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894075
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=42
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25801358
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