A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434059



Internal ID21396061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44340604..44345351hg38UCSC Ensembl
chr3:44382096..44386843hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg384748
hg194748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15751681
SamplesNB07
Known GenesTCAIM
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434059
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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