A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934474



Internal ID22709801
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 StatusM
Merged Variants
Supporting Variantsnssv17403058
Samples
Known GenesKLK9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934474
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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