A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582266



Internal ID20955337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95299809..95300758hg38UCSC Ensembl
chr15:95843038..95843987hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38950
hg19950
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239096
Samples
Known GenesLOC400456
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582266
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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