A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269477



Internal ID20478695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108190693..108194610hg38UCSC Ensembl
chr1:108733315..108737232hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg383918
hg193918
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739933
Supporting Variants
Samples
Known GenesSLC25A24
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269477
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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