A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434767



Internal ID21396769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142837864..142948863hg38UCSC Ensembl
chr6:143159001..143270000hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38111000
hg19111000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15749774
SamplesSMI041
Known GenesHIVEP2
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434767
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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