A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434896



Internal ID21396898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:256001..383000hg38UCSC Ensembl
chr6:256001..383000hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38127000
hg19127000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv671n172
Supporting Variantsnssv15745772, nssv15748259, nssv15747827, nssv15746821, nssv15753094, nssv15749421, nssv15751106
SamplesNB12, NB08, NB10, SMI041, NB11, NB07, NB09
Known GenesDUSP22
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434896
Frequency
Sample Size15
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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