A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17138459



Internal ID21456786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:8076813..8076890hg38UCSC Ensembl
chr4:8078540..8078617hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5581622
Supporting Variants
SamplesHG02587
Known GenesABLIM2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17138459
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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