A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16890857



Internal ID168078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155270000..155276587hg38UCSC Ensembl
chr1:155239791..155246378hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg386588
hg196588
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138309
Supporting Variants
Samples
Known GenesCLK2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16890857
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003686


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