A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17150876



Internal ID21503360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137946900..137946900hg38UCSC Ensembl
chr7:137631646..137631646hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5639146
Supporting Variants
SamplesNA19239
Known GenesCREB3L2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17150876
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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