A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5632436



Internal ID21580741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:113493104..113493104hg38UCSC Ensembl
chr7:113133159..113133159hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17143647
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5632436
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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