A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592137



Internal ID20965208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80627440..80629027hg38UCSC Ensembl
chr15:80919781..80921368hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg381588
hg191588
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2605n223
Supporting Variantsnssv18239772
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592137
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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