A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007407



Internal ID21916750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:44375930..44376617hg38UCSC Ensembl
chr6:44343667..44344354hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38688
hg19688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17560463
Samples
Known GenesSPATS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007407
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