A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434086



Internal ID21396088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73109850..73111849hg38UCSC Ensembl
chr3:73159001..73161000hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15749103, nssv15751525, nssv15749602, nssv15745804, nssv15751710, nssv15750616, nssv15746851
SamplesSMI034, NB08, MDQ010, SMI041, NB11, NB07, SMI018
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434086
Frequency
Sample Size15
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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