A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250647



Internal ID20817687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23299975..23300295hg38UCSC Ensembl
chr1:23626468..23626788hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555401
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250647
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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