A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17623318



Internal ID21815365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44312706..44312765hg38UCSC Ensembl
chr17:42390074..42390133hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6030752
Supporting Variants
Samples
Known GenesRUNDC3A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17623318
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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