A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443937



Internal ID21101490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5323596..5324010hg38UCSC Ensembl
chr11:5344826..5345240hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992200
Samples
Known GenesOR51B2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443937
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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