A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359515



Internal ID21017068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179069601..179076800hg38UCSC Ensembl
chr3:178787389..178794588hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg387200
hg197200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211510
Samples
Known GenesZMAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359515
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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