A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18051557



Internal ID20618597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:14331216..14331990hg38UCSC Ensembl
chr1:14657711..14658485hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38775
hg19775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322985
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18051557
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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