A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17134546



Internal ID21473493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:44016273..44025187hg38UCSC Ensembl
chr4:44018290..44027204hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg388915
hg198915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5573856
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17134546
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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