A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371730



Internal ID21029283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:6488901..6491000hg38UCSC Ensembl
chr3:6530588..6532687hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212959
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371730
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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