A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641606



Internal ID21589911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:55813547..55813547hg38UCSC Ensembl
chr7:55881240..55881240hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17146404
SamplesHG03065
Known GenesSEPT14
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641606
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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