A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656171



Internal ID21604476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16069538..16069538hg38UCSC Ensembl
chr19:16180348..16180348hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17103221
SamplesHG00731
Known GenesTPM4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656171
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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