A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384898



Internal ID21042451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:75862019..75875466hg38UCSC Ensembl
chr4:76783172..76796619hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3813448
hg1913448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18120232
Samples
Known GenesPPEF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384898
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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