A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880783



Internal ID22655753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:28988690..28991217hg38UCSC Ensembl
chr22:29384678..29387205hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg382528
hg192528
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482832, nssv17482831
Samples
Known GenesZNRF3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880783
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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