A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537680



Internal ID20911015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37595136..37597221hg38UCSC Ensembl
chr22:37991143..37993228hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg382086
hg192086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073917
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537680
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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