A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17521272



Internal ID21845631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:213567589..213567589hg38UCSC Ensembl
chr2:214432313..214432313hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6058865
Supporting Variants
Samples
Known GenesSPAG16
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17521272
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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