A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625091



Internal ID6665243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:966063..1001637hg38UCSC Ensembl
chr11:966063..1001637hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3835575
hg1935575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13992175, essv13992174, essv13992172, essv13992173, essv13992171, essv13992170, essv13992169
SamplesHG00596, HG00404, HG00266, HG00610, HG00634, HG00629, NA12272
Known GenesAP2A2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625091
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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