A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375555



Internal ID21033108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16663000..16666406hg38UCSC Ensembl
chr3:16704507..16707913hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg383407
hg193407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18098659
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375555
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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