A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250570



Internal ID20817610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63170635..63171210hg38UCSC Ensembl
chr1:63636306..63636881hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38576
hg19576
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555558
Supporting Variants
Samples
Known GenesLINC00466
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250570
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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