A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14233022



Internal ID2701068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:91229537..91313990hg38UCSC Ensembl
Innerchr11:91229593..91313934hg38UCSC Ensembl
Outerchr11:91229481..91314046hg38UCSC Ensembl
chr11:90962705..91047157hg19UCSC Ensembl
Innerchr11:90962761..91047101hg19UCSC Ensembl
Outerchr11:90962649..91047213hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3884454
hg1984453
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627243
Supporting Variants
SamplesHG02386
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14233022
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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