A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17126872



Internal ID21497501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:181329694..181330004hg38UCSC Ensembl
chr4:182250847..182251157hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5578930
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17126872
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