A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275979



Internal ID20843019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43830050..43830709hg38UCSC Ensembl
chr7:43869649..43870308hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38660
hg19660
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558366
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275979
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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