A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588900



Internal ID20961971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36980018..36980294hg38UCSC Ensembl
chr13:37554155..37554431hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237100
Samples
Known GenesALG5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588900
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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