A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5949710



Internal ID22725152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33916528..33919610hg38UCSC Ensembl
chr21:35288832..35291914hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg383083
hg193083
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17406967
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5949710
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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