A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626673



Internal ID6666823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65414755..65425077hg38UCSC Ensembl
Innerchr11:65414755..65425077hg38UCSC Ensembl
Outerchr11:65414680..65425129hg38UCSC Ensembl
chr11:65182226..65192548hg19UCSC Ensembl
Innerchr11:65182226..65192548hg19UCSC Ensembl
Outerchr11:65182151..65192600hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3810323
hg1910323
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14189790
SamplesHG01256
Known GenesNEAT1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626673
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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