A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879968



Internal ID22654938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:222720047..222720770hg38UCSC Ensembl
chr1:222893389..222894112hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38724
hg19724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17369418
Samples
Known GenesBROX
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879968
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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