A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274713



Internal ID20483931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:57322134..57322134hg38UCSC Ensembl
chr10:59081894..59081894hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4766688
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274713
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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