A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16903431



Internal ID3096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58739632..58739632hg38UCSC Ensembl
chr1:59205304..59205304hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5553392
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16903431
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.134324


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