A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17637321



Internal ID21829368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1602897..1602897hg38UCSC Ensembl
chr20:1583543..1583543hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6112648
Supporting Variants
Samples
Known GenesSIRPB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17637321
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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