A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274681



Internal ID20841721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:56047712..56048192hg38UCSC Ensembl
chr7:56115405..56115885hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38481
hg19481
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570402
Supporting Variants
Samples
Known GenesPSPH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274681
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer