A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594172



Internal ID20967243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43124474..43125025hg38UCSC Ensembl
chr15:43416672..43417223hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38552
hg19552
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2509n223
Supporting Variantsnssv18239556
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594172
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer