A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18049589



Internal ID20616629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:100463602..100464153hg38UCSC Ensembl
chr1:100929158..100929709hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg38552
hg19552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6325217
Supporting Variants
Samples
Known GenesCDC14A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18049589
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00112


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