A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584164



Internal ID20957235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63161837..63162272hg38UCSC Ensembl
chr15:63454036..63454471hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238765
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584164
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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