A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360974



Internal ID21018527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:152791331..152805027hg38UCSC Ensembl
chr3:152509120..152522816hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3813697
hg1913697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096742
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360974
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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