A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5607751



Internal ID21556056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183449645..183449645hg38UCSC Ensembl
chr3:183167433..183167433hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17139528
SamplesHG03683
Known GenesLINC00888
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5607751
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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