A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553296



Internal ID20926405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41064801..41066200hg38UCSC Ensembl
chr22:41460805..41462204hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073868
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553296
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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