A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5627770



Internal ID21576075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:78503566..78503566hg38UCSC Ensembl
chr7:78132883..78132883hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17140114
SamplesHG00732
Known GenesMAGI2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5627770
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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