A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767545



Internal ID20543405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:220466492..220466492hg38UCSC Ensembl
chr1:220639834..220639834hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276201
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767545
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