A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587307



Internal ID20960378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42196023..42247614hg38UCSC Ensembl
chr15:42488221..42539812hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3851592
hg1951592
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238985
Samples
Known GenesMIR627, TMEM87A, VPS39
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587307
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