A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323321



Internal ID20856438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21907943..21992809hg38UCSC Ensembl
chr1:22234436..22319302hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3884867
hg1984867
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202030
Samples
Known GenesCELA3B, HSPG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323321
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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