A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565592



Internal ID21513906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168458324..168458385hg38UCSC Ensembl
chr6:168859004..168859065hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17141168
SamplesHG03065
Known GenesSMOC2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565592
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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