A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370455



Internal ID21028008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:34289602..34290252hg38UCSC Ensembl
chr3:34331094..34331744hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38651
hg19651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100102
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370455
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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