A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5655959



Internal ID21604264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29702554..29702554hg38UCSC Ensembl
chr19:30193461..30193461hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38214
hg19214
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17104549
SamplesHG01596
Known GenesC19orf12
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5655959
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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