A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433044



Internal ID21395046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:222376921..222377774hg38UCSC Ensembl
chr1:222550263..222551116hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38854
hg19854
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv49n172
Supporting Variantsnssv15751056
SamplesBTQ016
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433044
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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