A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787083



Internal ID18827831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:85560815..85628886hg38UCSC Ensembl
Innerchr10:87320572..87388643hg19UCSC Ensembl
Innerchr10:87310552..87378623hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3868072
hg1968072
hg1868072
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891878
Supporting Variants
Samples
Known GenesGRID1, GRID1-AS1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787083
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