A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269833



Internal ID20479051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:115686863..115690220hg38UCSC Ensembl
chr1:116229484..116232841hg19UCSC Ensembl
Cytoband1p13.1
Allele length
AssemblyAllele length
hg383358
hg193358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744603
Supporting Variants
Samples
Known GenesVANGL1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269833
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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