A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435572



Internal ID21397574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81840766..81842765hg38UCSC Ensembl
chr8:82753001..82755000hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15751481
SamplesSMI034
Known GenesSNX16
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4435572
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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