A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575761



Internal ID20948832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58979462..58980067hg38UCSC Ensembl
chr15:59271661..59272266hg19UCSC Ensembl
Cytoband15q22.1
Allele length
AssemblyAllele length
hg38606
hg19606
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241186
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575761
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