A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637376



Internal ID21585681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:78202172..78202172hg38UCSC Ensembl
chr7:77831489..77831489hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153488
SamplesHG02587
Known GenesMAGI2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637376
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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