A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326566



Internal ID20859703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:54532855..54571278hg38UCSC Ensembl
chr1:54998528..55036951hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3838424
hg1938424
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201476
Samples
Known GenesACOT11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326566
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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