A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14317585



Internal ID4319401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132209430..132211574hg38UCSC Ensembl
Innerchr11:132209456..132211549hg38UCSC Ensembl
Outerchr11:132209405..132211600hg38UCSC Ensembl
chr11:132079324..132081468hg19UCSC Ensembl
Innerchr11:132079350..132081443hg19UCSC Ensembl
Outerchr11:132079299..132081494hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg382145
hg192145
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3628120
Supporting Variants
SamplesNA12717
Known GenesNTM
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14317585
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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