A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539039



Internal ID20912346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26098294..26109288hg38UCSC Ensembl
chr22:26494260..26505254hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3810995
hg1910995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073152
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539039
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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