A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17401652



Internal ID22459522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8058465..8058577hg38UCSC Ensembl
chr19:8123349..8123461hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5930568
Supporting Variants
Samples
Known GenesCCL25
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17401652
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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