A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272033



Internal ID20481251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:56100068..56100068hg38UCSC Ensembl
chr5:55395895..55395895hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4754829
Supporting Variants
Samples
Known GenesANKRD55
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272033
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