A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625157



Internal ID6665308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3882270..3885482hg38UCSC Ensembl
Innerchr11:3882270..3885482hg38UCSC Ensembl
Outerchr11:3881999..3885712hg38UCSC Ensembl
chr11:3903500..3906712hg19UCSC Ensembl
Innerchr11:3903500..3906712hg19UCSC Ensembl
Outerchr11:3903229..3906942hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383213
hg193213
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13997088
SamplesHG00525
Known GenesSTIM1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625157
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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