A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17140237



Internal ID21507656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107230013..107230013hg38UCSC Ensembl
chr7:106870458..106870458hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5633332
Supporting Variants
SamplesNA20509
Known GenesCOG5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17140237
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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