A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16903383



Internal ID3068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:55971642..55971642hg38UCSC Ensembl
chr1:56437315..56437315hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5542515
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16903383
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.317551


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