A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272952



Internal ID20839992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:124496585..124498655hg38UCSC Ensembl
chr7:124136639..124138709hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg382071
hg192071
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559450
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272952
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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