A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373888



Internal ID21031441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:7798105..7942353hg38UCSC Ensembl
chr3:7839792..7984040hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38144249
hg19144249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4785n223
Supporting Variantsnssv18105231
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373888
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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