A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17106076



Internal ID21461751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53921217..53921217hg38UCSC Ensembl
chr19:54424471..54424471hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38373
hg19373
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5651945
Supporting Variants
SamplesHG02818
Known GenesCACNG7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17106076
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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