A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589161



Internal ID20962232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60623893..60624999hg38UCSC Ensembl
chr13:61198027..61199133hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg381107
hg191107
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1861n223
Supporting Variantsnssv18229647
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589161
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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