A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18051512



Internal ID20618552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13527684..13530526hg38UCSC Ensembl
chr1:13854179..13857021hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg382843
hg192843
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317883
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18051512
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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