A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14317097



Internal ID4318913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131917641..131921538hg38UCSC Ensembl
Innerchr11:131917653..131921526hg38UCSC Ensembl
Outerchr11:131917629..131921550hg38UCSC Ensembl
chr11:131787535..131791432hg19UCSC Ensembl
Innerchr11:131787547..131791420hg19UCSC Ensembl
Outerchr11:131787523..131791444hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg383898
hg193898
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3628113
Supporting Variants
SamplesNA20813
Known GenesNTM
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14317097
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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