A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18108449



Internal ID20675489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:111334601..111348000hg38UCSC Ensembl
chr4:112255757..112269156hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3813400
hg1913400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6384119
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18108449
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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