A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641370



Internal ID21589675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99480291..99480291hg38UCSC Ensembl
chr7:99077914..99077914hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17158982
SamplesNA12878
Known GenesZNF789
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641370
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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