A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17106031



Internal ID21426838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5131563..5131563hg38UCSC Ensembl
chr19:5131574..5131574hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5645039
Supporting Variants
SamplesHG00731
Known GenesKDM4B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17106031
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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