A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17637502



Internal ID21829549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44311886..44311886hg38UCSC Ensembl
chr17:42389254..42389254hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6088157
Supporting Variants
Samples
Known GenesRUNDC3A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17637502
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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