A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007990



Internal ID21917333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:146049731..146058519hg38UCSC Ensembl
chr7:145746824..145755612hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg388789
hg198789
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17566544
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007990
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