A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549507



Internal ID20922668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45184993..45185709hg38UCSC Ensembl
chr22:45580874..45581590hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38717
hg19717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074926
Samples
Known GenesNUP50
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549507
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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