A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276797



Internal ID20843837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:84929855..84931232hg38UCSC Ensembl
chr7:84559171..84560548hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg381378
hg191378
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556862
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276797
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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