A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443474



Internal ID21101027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15936785..15962720hg38UCSC Ensembl
chr11:15958331..15984266hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3825936
hg1925936
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17989426
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443474
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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