A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248988



Internal ID20816028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244356923..244357592hg38UCSC Ensembl
chr1:244520225..244520894hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38670
hg19670
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551634
Supporting Variants
Samples
Known GenesC1orf100
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248988
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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