A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16264395



Internal ID20473613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:52064222..52064222hg38UCSC Ensembl
chr8:52976782..52976782hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4753232
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16264395
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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