A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432926



Internal ID21394928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11306328..11326476hg38UCSC Ensembl
chr1:11366385..11386533hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3820149
hg1920149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15747072
SamplesBTQ055
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432926
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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