A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784588



Internal ID19166351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:33766022..33792445hg38UCSC Ensembl
Innerchr21:35138326..35164749hg19UCSC Ensembl
Innerchr21:34060196..34086619hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3826424
hg1926424
hg1826424
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893407
Supporting Variants
Samples
Known GenesITSN1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784588
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