A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790766



Internal ID19179466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:126281817..127117455hg38UCSC Ensembl
Innerchr10:127970386..128915719hg19UCSC Ensembl
Innerchr10:127960376..128805709hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38835639
hg19945334
hg18845334
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891896
Supporting Variants
Samples
Known GenesADAM12, C10orf90, DOCK1, LINC00601
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=276
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790766
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer