A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16922774



Internal ID15939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:186469618..186489618hg38UCSC Ensembl
chr2:187334345..187354345hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3820001
hg1920001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5451738
Supporting Variants
Samples
Known GenesZC3H15
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16922774
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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