A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364187



Internal ID21021740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:83347388..83401575hg38UCSC Ensembl
chr3:83396539..83450726hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3854188
hg1954188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103429
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364187
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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