A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797897



Internal ID19165889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:105494795..105707657hg38UCSC Ensembl
Innerchr1:106037417..106250279hg19UCSC Ensembl
Innerchr1:105838940..106051802hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38212863
hg19212863
hg18212863
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893923
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=37
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797897
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