A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16898262



Internal ID172982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:227740862..227741026hg38UCSC Ensembl
chr1:227928563..227928727hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5450031
Supporting Variants
Samples
Known GenesSNAP47
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16898262
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000624


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