A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6457617



Internal ID8999100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128054361..128065525hg38UCSC Ensembl
chr11:127924256..127935420hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3811165
hg1911165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658124
Supporting Variants
SamplesHG00607
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6457617
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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