A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432818



Internal ID21394820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34801097..34805096hg38UCSC Ensembl
chr19:35292001..35296000hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg384000
hg194000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15745825, nssv15752004
SamplesMDQ010, MDQ025
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432818
Frequency
Sample Size15
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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