A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633651



Internal ID21581956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25247602..25247602hg38UCSC Ensembl
chr7:25287221..25287221hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17142420
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633651
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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