A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471987



Internal ID21129540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34625168..34625684hg38UCSC Ensembl
chr11:34646715..34647231hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38517
hg19517
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990856
Samples
Known GenesEHF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471987
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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