A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797328



Internal ID19162159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82316976..82351349hg38UCSC Ensembl
Innerchr10:84076732..84111105hg19UCSC Ensembl
Innerchr10:84066712..84101085hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3834374
hg1934374
hg1834374
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891872
Supporting Variants
Samples
Known GenesNRG3
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797328
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