A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800335



Internal ID19167352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:36800190..36808001hg38UCSC Ensembl
Innerchr10:37089118..37096929hg19UCSC Ensembl
Innerchr10:37129124..37136935hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg387812
hg197812
hg187812
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891784
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800335
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