A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17151336



Internal ID21495118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39419047..39419118hg38UCSC Ensembl
chr7:39458646..39458717hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5577524
Supporting Variants
SamplesNA19238
Known GenesPOU6F2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17151336
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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