A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432903



Internal ID21394905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9819399..9820570hg38UCSC Ensembl
chr19:9930075..9931246hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381172
hg191172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv362n172
Supporting Variantsnssv15749351
SamplesNB08
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432903
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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