A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571955



Internal ID20945026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71907618..71908323hg38UCSC Ensembl
chr9:74522534..74523239hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38706
hg19706
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280886
Samples
Known GenesABHD17B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571955
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