A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249020



Internal ID20816060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244868232..244868876hg38UCSC Ensembl
chr1:245031534..245032178hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38645
hg19645
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545262
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249020
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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