A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765657



Internal ID20541517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8216983..8216983hg38UCSC Ensembl
chr1:8277043..8277043hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38209
hg19209
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292070
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765657
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