A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332540



Internal ID20865712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:89278049..89304416hg38UCSC Ensembl
chr1:89743732..89770099hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3826368
hg1926368
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205216
Samples
Known GenesLOC729930
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332540
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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