A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454357



Internal ID21111910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1248028..1249745hg38UCSC Ensembl
chr11:1269258..1270975hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg381718
hg191718
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987842
Samples
Known GenesMUC5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454357
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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