A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580978



Internal ID20954049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:48245156..48245779hg38UCSC Ensembl
chr13:48819292..48819915hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg38624
hg19624
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228036
Samples
Known GenesITM2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580978
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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