A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585911



Internal ID20958982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83216614..83218643hg38UCSC Ensembl
chr15:83885366..83887395hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg382030
hg192030
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2609n223
Supporting Variantsnssv18240440
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585911
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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