A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751559



Internal ID20527419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101804299..101804299hg38UCSC Ensembl
chr8:102816527..102816527hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291172
Samples
Known GenesNCALD
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751559
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