A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791274



Internal ID18825876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5200060..5318770hg38UCSC Ensembl
Innerchr9:5200060..5318770hg19UCSC Ensembl
Innerchr9:5190060..5308770hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38118711
hg19118711
hg18118711
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891538
Supporting Variants
Samples
Known GenesINSL4, RLN2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=20
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791274
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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