A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15703213



Internal ID21375489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121055497..121055648hg38UCSC Ensembl
chr4:121976652..121976803hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4391429
Supporting Variants
Samples
Known GenesNDNF
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15703213
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0344828


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