A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17125936



Internal ID21502020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47976153..47976280hg38UCSC Ensembl
chr4:47978170..47978297hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569529
Supporting Variants
SamplesNA19239
Known GenesCNGA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17125936
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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