A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572150



Internal ID20945221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:134386496..134387031hg38UCSC Ensembl
chr5:133722187..133722722hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267310
Samples
Known GenesUBE2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572150
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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