A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052064



Internal ID20619104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15520971..15523437hg38UCSC Ensembl
chr1:15847466..15849932hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg382467
hg192467
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6323088
Supporting Variants
Samples
Known GenesCASP9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052064
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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