A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591876



Internal ID20964947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62195496..62196357hg38UCSC Ensembl
chr15:62487695..62488556hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38862
hg19862
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2561n223
Supporting Variantsnssv18238140
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591876
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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