A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15747620



Internal ID21391764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81840766..81844765hg38UCSC Ensembl
chr8:82753001..82757000hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg384000
hg194000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4435573
Supporting Variants
SamplesSMI018
Known GenesSNX16
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15747620
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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