A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5636372



Internal ID21584677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28838227..28838227hg38UCSC Ensembl
chr7:28877844..28877844hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150934
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5636372
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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