A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577413



Internal ID20950484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26249689..26250499hg38UCSC Ensembl
chr15:26494836..26495646hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38811
hg19811
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239407
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577413
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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