A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272956



Internal ID20839996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12471874..12471924hg38UCSC Ensembl
chr7:12511500..12511550hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555690
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272956
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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