A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16913933



Internal ID10042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:66533804..66534652hg38UCSC Ensembl
chr2:66760936..66761784hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38849
hg19849
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5436867
Supporting Variants
Samples
Known GenesMEIS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16913933
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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