A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878928



Internal ID22653895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26961176..26961570hg38UCSC Ensembl
chr1:27287667..27288061hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38395
hg19395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353891
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878928
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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