A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829200



Internal ID22604135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21993549..22002720hg38UCSC Ensembl
chr1:22320042..22329213hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg389172
hg199172
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469032, nssv17456045
Samples
Known GenesCELA3A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829200
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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