A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893204



Internal ID19184024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:119240639..119249781hg38UCSC Ensembl
Outerchr2:119240639..119249781hg38UCSC Ensembl
Innerchr2:119998215..120007357hg19UCSC Ensembl
Outerchr2:119998215..120007357hg19UCSC Ensembl
Innerchr2:119714685..119723827hg18UCSC Ensembl
Outerchr2:119714685..119723827hg18UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg389143
hg199143
hg189143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780673
Samples
Known GenesSTEAP3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893204
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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