A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17030414



Internal ID87983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16447578..16447669hg38UCSC Ensembl
chr10:16489577..16489668hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5483654
Supporting Variants
Samples
Known GenesPTER
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17030414
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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