A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5955949



Internal ID22731142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:25800836..25861699hg38UCSC Ensembl
chr21:27173147..27234010hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3860864
hg1960864
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1350n209
Supporting Variantsnssv17404647
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5955949
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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