A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577908



Internal ID20950979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27612680..27613616hg38UCSC Ensembl
chr13:28186817..28187753hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg38937
hg19937
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235913
Samples
Known GenesLNX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577908
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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