A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5608088



Internal ID21556393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57639800..57639800hg38UCSC Ensembl
chr3:57625527..57625527hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17135844
SamplesHG02818
Known GenesDENND6A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5608088
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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