A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16925693



Internal ID17878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:225520935..225521116hg38UCSC Ensembl
chr2:226385651..226385832hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557285
Supporting Variants
Samples
Known GenesNYAP2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16925693
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.025289


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