A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375159



Internal ID21032712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52018257..52047920hg38UCSC Ensembl
chr3:52052273..52081936hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg3829664
hg1929664
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209981
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375159
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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