A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432874



Internal ID21394876
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 StatusM
Merged Variantsdgv380n172
Supporting Variantsnssv15753734, nssv15752812, nssv15749147, nssv15753433, nssv15751073
SamplesNB12, SMI034, BTQ055, NB11, SMI018
Known GenesSBK2
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432874
Frequency
Sample Size15
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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