A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587925



Internal ID20960996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:26697425..26698162hg38UCSC Ensembl
chr12:26850358..26851095hg19UCSC Ensembl
Cytoband12p11.23
Allele length
AssemblyAllele length
hg38738
hg19738
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231990
Samples
Known GenesITPR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587925
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