A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17129649



Internal ID21465513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165019784..165020033hg38UCSC Ensembl
chr4:165940936..165941185hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38250
hg19250
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574223
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17129649
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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