A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537092



Internal ID20910432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:118458667..118506730hg38UCSC Ensembl
chr1:119001290..119049353hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3848064
hg1948064
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249880
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537092
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