A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17139222



Internal ID21501294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15350308..15350308hg38UCSC Ensembl
chr4:15351932..15351932hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38367
hg19367
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5622260
Supporting Variants
SamplesNA19239
Known GenesC1QTNF7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17139222
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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