A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16924174



Internal ID16882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:132899787..132953018hg38UCSC Ensembl
chr2:133657360..133710591hg19UCSC Ensembl
Cytoband2q21.2
Allele length
AssemblyAllele length
hg3853232
hg1953232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449720
Supporting Variants
Samples
Known GenesMIR7853, NCKAP5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16924174
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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