A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18110846



Internal ID20677886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:144261750..144262388hg38UCSC Ensembl
chr4:145182903..145183541hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38639
hg19639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6385574
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18110846
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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