A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052146



Internal ID20619186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:14636334..14638308hg38UCSC Ensembl
chr1:14962830..14964804hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg381975
hg191975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6316029
Supporting Variants
Samples
Known GenesKAZN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052146
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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