A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272021



Internal ID20481239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156328031..156328031hg38UCSC Ensembl
chr1:156297822..156297822hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4760634
Supporting Variants
Samples
Known GenesCCT3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272021
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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