A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628762



Internal ID21577067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107727434..107727434hg38UCSC Ensembl
chr7:107367879..107367879hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38579
hg19579
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153399
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628762
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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