A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563438



Internal ID20936509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:134162282..134163054hg38UCSC Ensembl
chr5:133497973..133498745hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38773
hg19773
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267287
Samples
Known GenesSKP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563438
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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