A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276037



Internal ID20843077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:45843017..45844004hg38UCSC Ensembl
chr7:45882616..45883603hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg38988
hg19988
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562577
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276037
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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