A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371375



Internal ID21028928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36586205..36643217hg38UCSC Ensembl
chr3:36627697..36684709hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3857013
hg1957013
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211176
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371375
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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