A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18055787



Internal ID20622827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19432954..19449434hg38UCSC Ensembl
chr1:19759448..19775928hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3816481
hg1916481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6323993
Supporting Variants
Samples
Known GenesCAPZB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18055787
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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