A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326782



Internal ID20859919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:243556240..243557233hg38UCSC Ensembl
chr1:243719542..243720535hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38994
hg19994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059566
Samples
Known GenesAKT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326782
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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