A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780890



Internal ID19172927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:177534370..178089493hg38UCSC Ensembl
Innerchr4:178455524..179010647hg19UCSC Ensembl
Innerchr4:178692518..179247641hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38555124
hg19555124
hg18555124
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894077
Supporting Variants
Samples
Known GenesLINC01098, LINC01099
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=123
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780890
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