A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642579



Internal ID21590884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128258665..128258665hg38UCSC Ensembl
chr7:127898718..127898718hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17147528
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642579
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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