A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16925910



Internal ID18028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:216691840..216692400hg38UCSC Ensembl
chr2:217556563..217557123hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38561
hg19561
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5451650
Supporting Variants
Samples
Known GenesIGFBP5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16925910
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000625


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