A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252767



Internal ID20819807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:94084069..94086854hg38UCSC Ensembl
chr1:94549625..94552410hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg382786
hg192786
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535830
Supporting Variants
Samples
Known GenesABCA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252767
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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