A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577520



Internal ID20950591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:49914847..49915530hg38UCSC Ensembl
chr12:50308630..50309313hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg38684
hg19684
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231242
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577520
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