A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537633



Internal ID20910969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27805102..27807366hg38UCSC Ensembl
chr22:28201090..28203354hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg382265
hg192265
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073226
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537633
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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