A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276004



Internal ID20843044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44816711..44817612hg38UCSC Ensembl
chr7:44856310..44857211hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556875
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276004
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00021


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