A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583445



Internal ID20956516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92476938..92481944hg38UCSC Ensembl
chr15:93020168..93025174hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg385007
hg195007
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239054
Samples
Known GenesC15orf32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583445
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