A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868921



Internal ID22643856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108855306..108855678hg38UCSC Ensembl
chr1:109397928..109398300hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38373
hg19373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359289
Samples
Known GenesAKNAD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868921
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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