A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538184



Internal ID20911507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:178839464..178991817hg38UCSC Ensembl
chr1:178808599..178960952hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38152354
hg19152354
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv450n223
Supporting Variantsnssv18247812
Samples
Known GenesANGPTL1, RALGPS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538184
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