A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760634



Internal ID20536494
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 StatusM
Merged Variants
Supporting Variantsnssv16272021
Samples
Known GenesCCT3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760634
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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