A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458081



Internal ID21115634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:50808227..50819936hg38UCSC Ensembl
chr11:50767398..50779107hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg3811710
hg1911710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992166
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458081
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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