A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267039



Internal ID20834079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:71698586..71699246hg38UCSC Ensembl
chr5:70994413..70995073hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38661
hg19661
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563966
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267039
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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