A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638191



Internal ID21586496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21248154..21248154hg38UCSC Ensembl
chr7:21287773..21287773hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150416
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638191
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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