A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6044527



Internal ID21953809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45307094..45307195hg38UCSC Ensembl
chr19:45810352..45810453hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619212
Samples
Known GenesCKM
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6044527
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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