A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5961287



Internal ID22736246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:37335159..37339552hg38UCSC Ensembl
chr21:38707461..38711854hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg384394
hg194394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392130
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5961287
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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