A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469931



Internal ID21127484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32317034..32319427hg38UCSC Ensembl
chr11:32338580..32340973hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg382394
hg192394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990616
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469931
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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