A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625876



Internal ID7012710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33258958..33264319hg38UCSC Ensembl
Innerchr11:33259001..33264276hg38UCSC Ensembl
Outerchr11:33258915..33264362hg38UCSC Ensembl
chr11:33280504..33285865hg19UCSC Ensembl
Innerchr11:33280547..33285822hg19UCSC Ensembl
Outerchr11:33280461..33285908hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg385362
hg195362
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14085506
SamplesNA19063
Known GenesHIPK3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625876
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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