A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014602



Internal ID21923945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135761453..135761537hg38UCSC Ensembl
chr7:135446201..135446285hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558478
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014602
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