A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263373



Internal ID20472591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:213152319..213152371hg38UCSC Ensembl
chr1:213325662..213325714hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743693
Supporting Variants
Samples
Known GenesRPS6KC1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263373
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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