A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17156326



Internal ID21482151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28426928..28426928hg38UCSC Ensembl
chr7:28466547..28466547hg19UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg38493
hg19493
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5626184
Supporting Variants
SamplesHG03732
Known GenesCREB5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17156326
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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