A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586008



Internal ID21534557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10101606..10103890hg38UCSC Ensembl
chr19:10212282..10214566hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382285
hg192285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17103109
SamplesHG00171
Known GenesANGPTL6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586008
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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