A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326759



Internal ID20859896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:232221722..232225403hg38UCSC Ensembl
chr1:232357468..232361149hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg383682
hg193682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058729
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326759
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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