A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17488911



Internal ID22546829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43035807..43046044hg38UCSC Ensembl
chr21:44455917..44466154hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3810238
hg1910238
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5879472
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17488911
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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