A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392267



Internal ID21049820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:135925101..135952000hg38UCSC Ensembl
chr4:136846256..136873155hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3826900
hg1926900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210843
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392267
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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