A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14317051



Internal ID4318867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131726291..131727357hg38UCSC Ensembl
Innerchr11:131726300..131727348hg38UCSC Ensembl
Outerchr11:131726282..131727366hg38UCSC Ensembl
chr11:131596185..131597251hg19UCSC Ensembl
Innerchr11:131596194..131597242hg19UCSC Ensembl
Outerchr11:131596176..131597260hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg381067
hg191067
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3628109
Supporting Variants
SamplesNA18517
Known GenesNTM
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14317051
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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