A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042776



Internal ID21952088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18892390..18892532hg38UCSC Ensembl
chr19:19003199..19003341hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636577
Samples
Known GenesCERS1, GDF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042776
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