A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381717



Internal ID21039270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:75859454..75861702hg38UCSC Ensembl
chr4:76780607..76782855hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg382249
hg192249
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212379
Samples
Known GenesPPEF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381717
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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