A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16903684



Internal ID3274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35497235..35504338hg38UCSC Ensembl
chr1:35962836..35969939hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg387104
hg197104
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5420692
Supporting Variants
Samples
Known GenesKIAA0319L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16903684
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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