A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591453



Internal ID20964524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:94586033..94586265hg38UCSC Ensembl
chr13:95238287..95238519hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225058
Samples
Known GenesTGDS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591453
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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