A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548474



Internal ID20921660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33100334..33100867hg38UCSC Ensembl
chr1:33565935..33566468hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38534
hg19534
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250879
Samples
Known GenesADC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548474
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