A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565962



Internal ID21514281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165575781..165575902hg38UCSC Ensembl
chr6:165989269..165989390hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17140927
SamplesHG02011
Known GenesPDE10A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565962
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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