A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891538



Internal ID18839248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5218524..5291710hg38UCSC Ensembl
Outerchr9:5200060..5324922hg38UCSC Ensembl
Innerchr9:5218524..5291710hg19UCSC Ensembl
Outerchr9:5200060..5324922hg19UCSC Ensembl
Innerchr9:5208524..5281710hg18UCSC Ensembl
Outerchr9:5190060..5314922hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38124863
hg19124863
hg18124863
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788515, essv25788596, essv25788337, essv25788616, essv25788609, essv25791274, essv25788753, essv25788579
Samples
Known GenesINSL4, RLN2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891538
Frequency
Sample Size3017
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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