A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15751073



Internal ID21392029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55530497..55530780hg38UCSC Ensembl
chr19:56041864..56042147hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432874
Supporting Variants
SamplesSMI034
Known GenesSBK2
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15751073
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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