A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17605271



Internal ID21797318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66491246..66491246hg38UCSC Ensembl
chr15:66783584..66783584hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6095344
Supporting Variants
Samples
Known GenesMAP2K1, SNAPC5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17605271
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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