A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390510



Internal ID21048063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145614201..145622900hg38UCSC Ensembl
chr4:146535353..146544052hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg388700
hg198700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212018
Samples
Known GenesMMAA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390510
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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