A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468686



Internal ID21126239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34224133..34275725hg38UCSC Ensembl
chr11:34245680..34297272hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3851593
hg1951593
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990838
Samples
Known GenesABTB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468686
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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