A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358596



Internal ID21016149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4143524..4241717hg38UCSC Ensembl
chr3:4185208..4283401hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3898194
hg1998194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4775n223
Supporting Variantsnssv18099815
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358596
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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