A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788827



Internal ID18826064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46400646..46587950hg38UCSC Ensembl
Innerchr10:46961667..47149117hg19UCSC Ensembl
Innerchr10:46381673..46569123hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38187305
hg19187451
hg18187451
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891799
Supporting Variants
Samples
Known GenesGPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R, SYT15
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788827
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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