A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641334



Internal ID21589639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168835647..168835647hg38UCSC Ensembl
chr4:169756798..169756798hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17129509
SamplesHG00731
Known GenesPALLD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641334
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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