A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14221681



Internal ID3910259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:85891174..85910446hg38UCSC Ensembl
Innerchr11:85891674..85909946hg38UCSC Ensembl
Outerchr11:85890174..85911446hg38UCSC Ensembl
chr11:85602217..85621489hg19UCSC Ensembl
Innerchr11:85602717..85620989hg19UCSC Ensembl
Outerchr11:85601217..85622489hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3819273
hg1919273
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627078
Supporting Variants
SamplesHG03565
Known GenesCCDC83
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14221681
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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