A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17523677



Internal ID21848036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:118142056..118142056hg38UCSC Ensembl
chr1:118684679..118684679hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6057792
Supporting Variants
Samples
Known GenesSPAG17
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17523677
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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