A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249764



Internal ID20816804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52924245..52924437hg38UCSC Ensembl
chr1:53389917..53390109hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38193
hg19193
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555096
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249764
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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