A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17403058



Internal ID22460928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51005496..51007808hg38UCSC Ensembl
chr19:51508752..51511064hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg382313
hg192313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5934474
Supporting Variants
Samples
Known GenesKLK9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17403058
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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