A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18273775



Internal ID20840815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155879513..155896835hg38UCSC Ensembl
chr7:155672207..155689529hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3817323
hg1917323
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562633
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18273775
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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