A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580882



Internal ID20953953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60514316..60514727hg38UCSC Ensembl
chr17:58591677..58592088hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38412
hg19412
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243089
Samples
Known GenesAPPBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580882
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