A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547963



Internal ID20921162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12046801..12061900hg38UCSC Ensembl
chr1:142567802..142582894hg19UCSC Ensembl
Cytoband1q12
Allele length
AssemblyAllele length
hg3815100
hg1915093
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203852
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547963
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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