A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324364



Internal ID20857490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67500118..67501736hg38UCSC Ensembl
chr1:67965801..67967419hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg381619
hg191619
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204315
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324364
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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