A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249027



Internal ID20816067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244908755..244909420hg38UCSC Ensembl
chr1:245072057..245072722hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38666
hg19666
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540812
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249027
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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