A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381866



Internal ID21039419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:63109382..64064623hg38UCSC Ensembl
chr4:63975100..64930341hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38955242
hg19955242
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210946
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381866
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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