A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360029



Internal ID21017582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71816065..71824250hg38UCSC Ensembl
chr3:71865216..71873401hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg388186
hg198186
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208694
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360029
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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