A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18059621



Internal ID20626661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244232060..244235346hg38UCSC Ensembl
chr1:244395362..244398648hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg383287
hg193287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6316675
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18059621
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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