A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627511



Internal ID7014339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101506235..101512986hg38UCSC Ensembl
Innerchr11:101506235..101512986hg38UCSC Ensembl
Outerchr11:101506093..101513161hg38UCSC Ensembl
chr11:101376966..101383717hg19UCSC Ensembl
Innerchr11:101376966..101383717hg19UCSC Ensembl
Outerchr11:101376824..101383892hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg386752
hg196752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14252144, essv14252141, essv14252143, essv14252145, essv14252142, essv14252146, essv14252147
SamplesHG02895, HG01048, NA19247, NA19390, NA19037, NA19093, NA19430
Known GenesTRPC6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627511
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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