A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274355



Internal ID20841395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:13819202..13820173hg38UCSC Ensembl
chr7:13858827..13859798hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg38972
hg19972
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555657
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274355
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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