A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625439



Internal ID6665586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15595815..15597827hg38UCSC Ensembl
Innerchr11:15595815..15597827hg38UCSC Ensembl
Outerchr11:15595597..15598107hg38UCSC Ensembl
chr11:15617361..15619373hg19UCSC Ensembl
Innerchr11:15617361..15619373hg19UCSC Ensembl
Outerchr11:15617143..15619653hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg382013
hg192013
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14034666
SamplesHG00536
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625439
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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