A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435259



Internal ID21397261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26954543..26955461hg38UCSC Ensembl
chr7:26994162..26995080hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38919
hg19919
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15748563
SamplesMDQ025
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4435259
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer