A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17548442



Internal ID21872797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183287176..183287176hg38UCSC Ensembl
chr3:183004964..183004964hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6068179
Supporting Variants
Samples
Known GenesMCF2L2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17548442
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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