A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5627753



Internal ID21576058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:41183098..41183098hg38UCSC Ensembl
chr7:41222696..41222696hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150324
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5627753
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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