A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584039



Internal ID20957110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:33202711..33203464hg38UCSC Ensembl
chr15:33494912..33495665hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38754
hg19754
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239513
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584039
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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