A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567617



Internal ID20940688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69212503..69491363hg38UCSC Ensembl
chr4:70078221..70357081hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38278861
hg19278861
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5317n223
Supporting Variantsnssv18265920
Samples
Known GenesUGT2B11, UGT2B28, UGT2B4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567617
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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