A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17539660



Internal ID21864015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49913643..49913643hg38UCSC Ensembl
chr3:49951076..49951076hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6065249
Supporting Variants
Samples
Known GenesMON1A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17539660
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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