A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878948



Internal ID22653915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33694690..33702969hg38UCSC Ensembl
chr21:35066995..35075274hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg388280
hg198280
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480311
Samples
Known GenesITSN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878948
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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