A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554798



Internal ID20927889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:29697854..29699608hg38UCSC Ensembl
chr22:30093843..30095597hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg381755
hg191755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073029
Samples
Known GenesNF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554798
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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