A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591703



Internal ID20964774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27178856..27179821hg38UCSC Ensembl
chr13:27752993..27753958hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38966
hg19966
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1784n223
Supporting Variantsnssv18229804
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591703
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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