A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17136876



Internal ID21469371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:4396655..4396722hg38UCSC Ensembl
chr4:4398382..4398449hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5572901
Supporting Variants
SamplesHG03125
Known GenesNSG1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17136876
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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