A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869315



Internal ID22644250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44863330..44874252hg38UCSC Ensembl
chr21:46283245..46294167hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3810923
hg1910923
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480922
Samples
Known GenesPTTG1IP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869315
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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