A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537871



Internal ID20911200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50757501..50758000hg38UCSC Ensembl
chr22:51195929..51196428hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074647
Samples
Known GenesRPL23AP82
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537871
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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