A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251018



Internal ID20818058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35784605..35784885hg38UCSC Ensembl
chr1:36250206..36250486hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548556
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251018
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