A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052055



Internal ID20619095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15507190..15514366hg38UCSC Ensembl
chr1:15833685..15840861hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg387177
hg197177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6323282
Supporting Variants
Samples
Known GenesCASP9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052055
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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