A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16911329



Internal ID8320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:28384434..28388720hg38UCSC Ensembl
chr2:28607301..28611587hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg384287
hg194287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5452674
Supporting Variants
Samples
Known GenesFLJ31356
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16911329
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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