A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585681



Internal ID20958752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8973174..8974445hg38UCSC Ensembl
chr12:9125770..9127041hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg381272
hg191272
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229654
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585681
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