A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17128406



Internal ID21497732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71158113..71158113hg38UCSC Ensembl
chr3:71207264..71207264hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604797
Supporting Variants
SamplesNA19238
Known GenesFOXP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17128406
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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