A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573882



Internal ID20946953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39750998..39751581hg38UCSC Ensembl
chr4:39752618..39753201hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38584
hg19584
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265188
Samples
Known GenesUBE2K
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573882
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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