A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581501



Internal ID20954572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:93115534..93486112hg38UCSC Ensembl
chr15:93658763..94029341hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38370579
hg19370579
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239068
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581501
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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