A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610385



Internal ID21802432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:38049984..38049984hg38UCSC Ensembl
chr14:38519189..38519189hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6087928
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610385
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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