A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17106046



Internal ID21474881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5146028..5146098hg38UCSC Ensembl
chr19:5146039..5146109hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591122
Supporting Variants
SamplesHG03371
Known GenesKDM4B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17106046
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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