A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4392865



Internal ID21383895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15841264..15844393hg38UCSC Ensembl
chr7:15880889..15884018hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg383130
hg193130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15704054
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4392865
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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