A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6199283



Internal ID9140521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:60805116..60806879hg38UCSC Ensembl
Outerchr11:60805079..60806929hg38UCSC Ensembl
Innerchr11:60572589..60574352hg19UCSC Ensembl
Outerchr11:60572552..60574402hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg381851
hg191851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2660563
Supporting Variants
SamplesHG01187
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6199283
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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