A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16903514



Internal ID3153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:29769382..30451469hg38UCSC Ensembl
chr1:30242229..30924316hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38682088
hg19682088
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425856
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16903514
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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