A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551947



Internal ID20925079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40883897..40886565hg38UCSC Ensembl
chr22:41279901..41282569hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg382669
hg192669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073854
Samples
Known GenesXPNPEP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551947
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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