A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373511



Internal ID21031064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31321546..31324931hg38UCSC Ensembl
chr3:31363038..31366423hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg383386
hg193386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099324
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373511
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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