A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17480301



Internal ID22538204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32300267..32305547hg38UCSC Ensembl
chr21:33672578..33677858hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg385281
hg195281
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880602
Supporting Variants
Samples
Known GenesMRAP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17480301
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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