A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752953



Internal ID20528813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38930747..38930747hg38UCSC Ensembl
chr17:37087000..37087000hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289920
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752953
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