A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361302



Internal ID21018855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:145721610..145779463hg38UCSC Ensembl
chr3:145439397..145497250hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3857854
hg1957854
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18095913
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361302
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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