A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052449



Internal ID20619489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16029027..16039616hg38UCSC Ensembl
chr1:16355522..16366111hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3810590
hg1910590
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331075
Supporting Variants
Samples
Known GenesCLCNKA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052449
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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