A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828055



Internal ID22602990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159044225..159049138hg38UCSC Ensembl
chr1:159014015..159018928hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg384914
hg194914
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467284, nssv17467101
Samples
Known GenesIFI16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828055
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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