A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252020



Internal ID20819060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9138226..9138701hg38UCSC Ensembl
chr1:9198285..9198760hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38476
hg19476
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536244
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252020
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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