A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539874



Internal ID20913169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38040606..38068404hg38UCSC Ensembl
chr22:38436613..38464411hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3827799
hg1927799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204643
Samples
Known GenesPICK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539874
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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