A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14317251



Internal ID4319067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132053654..132060279hg38UCSC Ensembl
chr11:131923548..131930173hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg386626
hg196626
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3628116
Supporting Variants
SamplesHG01085
Known GenesNTM
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14317251
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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