A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375315



Internal ID21032868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128691301..128696900hg38UCSC Ensembl
chr3:128410144..128415743hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5015n223
Supporting Variantsnssv18093185
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375315
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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