A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250960



Internal ID20818000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:41066787..41067294hg38UCSC Ensembl
chr1:41532459..41532966hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38508
hg19508
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542112
Supporting Variants
Samples
Known GenesSCMH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250960
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