A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567971



Internal ID20941042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:67693987..67694394hg38UCSC Ensembl
chr4:68559705..68560112hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38408
hg19408
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265271
Samples
Known GenesUBA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567971
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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