A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871181



Internal ID22646118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43029741..43036207hg38UCSC Ensembl
chr21:44449851..44456317hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg386467
hg196467
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480905
Samples
Known GenesPKNOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871181
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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