A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327782



Internal ID20860924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:243651728..243656783hg38UCSC Ensembl
chr1:243815030..243820085hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg385056
hg195056
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200649
Samples
Known GenesAKT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327782
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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