A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577698



Internal ID20950769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45243585..45244074hg38UCSC Ensembl
chr15:45535783..45536272hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38490
hg19490
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2527n223
Supporting Variantsnssv18240291
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577698
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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