A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577246



Internal ID20950317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:59600626..59987959hg38UCSC Ensembl
chr17:57677987..58065320hg19UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg38387334
hg19387334
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243772
Samples
Known GenesCLTC, DHX40, MIR21, PTRH2, RNFT1, RPS6KB1, TBC1D3P1-DHX40P1, TUBD1, VMP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577246
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