A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249472



Internal ID20816512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:182373963..182374946hg38UCSC Ensembl
chr1:182343098..182344081hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38984
hg19984
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550397
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249472
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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