A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276876



Internal ID20843916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90465771..90466504hg38UCSC Ensembl
chr7:90095085..90095818hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38734
hg19734
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570622
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276876
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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