A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269377



Internal ID20836417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151273756..151274371hg38UCSC Ensembl
chr6:151594891..151595506hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38616
hg19616
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564023
Supporting Variants
Samples
Known GenesAKAP12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269377
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer