A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469032



Internal ID22526922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21993549..22002720hg38UCSC Ensembl
chr1:22320042..22329213hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg389172
hg199172
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829200
Supporting Variants
Samples
Known GenesCELA3A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469032
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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