A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874416



Internal ID22649368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39063222..39068653hg38UCSC Ensembl
chr22:39459227..39464658hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg385432
hg195432
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482962
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874416
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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