A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540246



Internal ID20913538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26656984..26661963hg38UCSC Ensembl
chr22:27052948..27057927hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg384980
hg194980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073174
Samples
Known GenesMIAT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540246
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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