A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575722



Internal ID20948793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:46739091..46739953hg38UCSC Ensembl
chr17:44816457..44817319hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38863
hg19863
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242404
Samples
Known GenesNSF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575722
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