A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544126



Internal ID20917365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31052664..31057707hg38UCSC Ensembl
chr22:31448650..31453693hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg385044
hg195044
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205009
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544126
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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