A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587659



Internal ID20960730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95885394..95886328hg38UCSC Ensembl
chr10:97645151..97646085hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38935
hg19935
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236949
Samples
Known GenesENTPD1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587659
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