A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18246992



Internal ID20814032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:102140961..102146140hg38UCSC Ensembl
chr1:102606517..102611696hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg385180
hg195180
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536107
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18246992
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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