A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517758



Internal ID21842117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:53086992..53086992hg38UCSC Ensembl
chr1:53552664..53552664hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6048881
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17517758
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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