A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577958



Internal ID20951029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76532709..76533589hg38UCSC Ensembl
chr17:74528791..74529671hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38881
hg19881
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243202
Samples
Known GenesCYGB, PRCD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577958
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