A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547290



Internal ID20920492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:22945580..22946073hg38UCSC Ensembl
chr1:23272073..23272566hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38494
hg19494
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250328
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547290
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