A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364096



Internal ID21021649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4054633..4136813hg38UCSC Ensembl
chr3:4096317..4178497hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3882181
hg1982181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099148
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364096
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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