A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249281



Internal ID20816321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:220764185..220764747hg38UCSC Ensembl
chr1:220937527..220938089hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38563
hg19563
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539689
Supporting Variants
Samples
Known GenesMARC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249281
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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