A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18051997



Internal ID20619037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153787273..153795864hg38UCSC Ensembl
chr1:153759749..153768340hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg388592
hg198592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6324355
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18051997
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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