A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371837



Internal ID21029390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4064909..4107601hg38UCSC Ensembl
chr3:4106593..4149285hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3842693
hg1942693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4767n223
Supporting Variantsnssv18099153
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371837
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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