A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328592



Internal ID20861740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:243535400..243536862hg38UCSC Ensembl
chr1:243698702..243700164hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg381463
hg191463
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059564
Samples
Known GenesAKT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328592
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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