A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5564811



Internal ID21513118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160474442..160474505hg38UCSC Ensembl
chr5:159901449..159901512hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17135056
SamplesHG03065
Known GenesMIR3142
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5564811
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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