A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641125



Internal ID21589430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103178075..103178075hg38UCSC Ensembl
chr7:102818522..102818522hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17147365
SamplesNA19239
Known GenesDPY19L2P2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641125
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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