A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663995



Internal ID21612300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54161382..54161382hg38UCSC Ensembl
chr19:54665118..54665118hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17106203
SamplesHG01114
Known GenesTMC4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663995
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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