A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14168552



Internal ID5137725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56804027..56819915hg38UCSC Ensembl
Innerchr11:56804027..56819915hg38UCSC Ensembl
Outerchr11:56803527..56820415hg38UCSC Ensembl
chr11:56571503..56587391hg19UCSC Ensembl
Innerchr11:56571503..56587391hg19UCSC Ensembl
Outerchr11:56571003..56587891hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3815889
hg1915889
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626497
Supporting Variants
SamplesNA18571
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14168552
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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