A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332080



Internal ID20865249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:232309683..232368271hg38UCSC Ensembl
chr1:232445429..232504017hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg3858589
hg1958589
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058735
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332080
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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