A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755630



Internal ID20531490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:67831003..67831003hg38UCSC Ensembl
chr8:68743238..68743238hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285865
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755630
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