A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372587



Internal ID21030140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4047010..4109380hg38UCSC Ensembl
chr3:4088694..4151064hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3862371
hg1962371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099142
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372587
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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