A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011879



Internal ID21921222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87345722..87346387hg38UCSC Ensembl
chr7:86975038..86975703hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38666
hg19666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558101
Samples
Known GenesCROT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011879
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