A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577588



Internal ID20950659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91994508..92026504hg38UCSC Ensembl
chr13:92646761..92678757hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3831997
hg1931997
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236849
Samples
Known GenesGPC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577588
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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