A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5631726



Internal ID21580031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:924140..924140hg38UCSC Ensembl
chr7:963776..963776hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38669
hg19669
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17147947
SamplesHG00732
Known GenesADAP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5631726
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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