A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14237710



Internal ID4239526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93327732..93332073hg38UCSC Ensembl
Innerchr11:93327732..93332073hg38UCSC Ensembl
Outerchr11:93327646..93332280hg38UCSC Ensembl
chr11:93060898..93065239hg19UCSC Ensembl
Innerchr11:93060898..93065239hg19UCSC Ensembl
Outerchr11:93060812..93065446hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg384342
hg194342
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627290
Supporting Variants
SamplesHG03808
Known GenesCCDC67
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14237710
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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