A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388923



Internal ID21046476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:64648157..64685280hg38UCSC Ensembl
chr4:65513875..65550998hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3837124
hg1937124
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211574
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388923
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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