A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16900210



Internal ID934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25382500..25399265hg38UCSC Ensembl
chr1:25708991..25725756hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3816766
hg1916766
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5419322
Supporting Variants
Samples
Known GenesRHCE
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16900210
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.01154


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