A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18054060



Internal ID20621100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:178619298..178628946hg38UCSC Ensembl
chr1:178588433..178598081hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg389649
hg199649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6325526
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18054060
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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