A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250022



Internal ID20817062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20748478..20749545hg38UCSC Ensembl
chr1:21074971..21076038hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg381068
hg191068
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549417
Supporting Variants
Samples
Known GenesHP1BP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250022
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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