A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432821



Internal ID21394823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38735651..38736476hg38UCSC Ensembl
chr19:39226291..39227116hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38826
hg19826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15746715
SamplesSMI041
Known GenesCAPN12
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432821
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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