A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432051



Internal ID21394053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102761707..102762933hg38UCSC Ensembl
chr14:103228044..103229270hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg381227
hg191227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv247n172
Supporting Variantsnssv15752862
SamplesMDQ010
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432051
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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