A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434405



Internal ID21396407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:67397283..67402282hg38UCSC Ensembl
chr4:68263001..68268000hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15753494
SamplesBTQ038
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434405
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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