A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755629



Internal ID20531489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:21001006..21001006hg38UCSC Ensembl
chr2:21223878..21223878hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38204
hg19204
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288895
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755629
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