A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788337



Internal ID18825137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5200060..5324922hg38UCSC Ensembl
Innerchr9:5200060..5324922hg19UCSC Ensembl
Innerchr9:5190060..5314922hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38124863
hg19124863
hg18124863
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)essv25788337
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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