A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5619351



Internal ID21567656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:74176270..74176270hg38UCSC Ensembl
chr2:74403397..74403397hg19UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17113637
SamplesHG00731
Known GenesMOB1A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5619351
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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