A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893776



Internal ID19184596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:136388707..136581890hg38UCSC Ensembl
Outerchr3:136388707..136581890hg38UCSC Ensembl
Innerchr3:136107549..136300732hg19UCSC Ensembl
Outerchr3:136107549..136300732hg19UCSC Ensembl
Innerchr3:137590239..137783422hg18UCSC Ensembl
Outerchr3:137590239..137783422hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38193184
hg19193184
hg18193184
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784845
Samples
Known GenesSTAG1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893776
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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