A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6052934



Internal ID21962167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:64060000..64060000hg38UCSC Ensembl
chr2:64287134..64287134hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522571
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6052934
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer