A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330437



Internal ID20863594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:232744422..232765823hg38UCSC Ensembl
chr1:232880168..232901569hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg3821402
hg1921402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058759
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330437
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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