A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249003



Internal ID20816043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244669594..244670006hg38UCSC Ensembl
chr1:244832896..244833308hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38413
hg19413
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537137
Supporting Variants
Samples
Known GenesDESI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249003
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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