A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17529312



Internal ID21853669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:121225771..121225887hg38UCSC Ensembl
chr2:121983347..121983463hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5986076
Supporting Variants
Samples
Known GenesTFCP2L1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17529312
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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