A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390266



Internal ID21047819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:177185801..177248300hg38UCSC Ensembl
chr4:178106955..178169454hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3862500
hg1962500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212789
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390266
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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