A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542895



Internal ID20916146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31923265..31927112hg38UCSC Ensembl
chr22:32319251..32323098hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg383848
hg193848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073758
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542895
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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