A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250025



Internal ID20817065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20757437..20758146hg38UCSC Ensembl
chr1:21083930..21084639hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38710
hg19710
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541246
Supporting Variants
Samples
Known GenesHP1BP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250025
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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