A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274140



Internal ID20483358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71834938..71834938hg38UCSC Ensembl
chr10:73594695..73594695hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763904
Supporting Variants
Samples
Known GenesPSAP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274140
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