A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384676



Internal ID21042229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:75881359..75903291hg38UCSC Ensembl
chr4:76802512..76824444hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3821933
hg1921933
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212381
Samples
Known GenesPPEF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384676
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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