A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045061



Internal ID21954331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7870337..7870419hg38UCSC Ensembl
chr19:7935223..7935305hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617624
Samples
Known GenesFLJ22184
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045061
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