A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571320



Internal ID20944391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:131898260..131923684hg38UCSC Ensembl
chr5:131233953..131259377hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3825425
hg1925425
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267942
Samples
Known GenesLOC728637
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571320
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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