A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17482814



Internal ID22540720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27363156..27378107hg38UCSC Ensembl
chr22:27759117..27774068hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3814952
hg1914952
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877699
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17482814
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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