A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585472



Internal ID20958543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37036389..37037016hg38UCSC Ensembl
chr13:37610526..37611153hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38628
hg19628
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1803n223
Supporting Variantsnssv18225016
Samples
Known GenesSUPT20H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585472
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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