A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467101



Internal ID22524993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159044225..159049138hg38UCSC Ensembl
chr1:159014015..159018928hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg384914
hg194914
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828055
Supporting Variants
Samples
Known GenesIFI16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467101
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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