A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704159



Internal ID21376435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:67655987..67656060hg38UCSC Ensembl
chr7:67120974..67121047hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4392959
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704159
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.727011


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