A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581764



Internal ID20954835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:105633365..105833042hg38UCSC Ensembl
chr13:106285714..106485391hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg38199678
hg19199678
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220684
Samples
Known GenesLINC00343
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581764
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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