A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393770



Internal ID21051323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:43844701..43849300hg38UCSC Ensembl
chr4:43846718..43851317hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg384600
hg194600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213666
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393770
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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