A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547866



Internal ID20921066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:48870950..48887794hg38UCSC Ensembl
chr22:49266762..49283606hg19UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg3816845
hg1916845
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205679
Samples
Known GenesLOC100128946
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547866
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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