A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18115719



Internal ID20682759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169877462..169882140hg38UCSC Ensembl
chr4:170798613..170803291hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg384679
hg194679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6394085
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18115719
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00054


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