A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626782



Internal ID6666930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71538088..71562989hg38UCSC Ensembl
chr11:71249134..71274035hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3824902
hg1924902
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14210474
SamplesHG02084
Known GenesKRTAP5-8, KRTAP5-9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626782
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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