A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277225



Internal ID20486443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:55296727..55296727hg38UCSC Ensembl
chr18:52963958..52963958hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758526
Supporting Variants
Samples
Known GenesTCF4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277225
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer