A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577427



Internal ID20950498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:82300839..82301732hg38UCSC Ensembl
chr13:82874974..82875867hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38894
hg19894
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234935
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577427
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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