A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5622260



Internal ID21570565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15350308..15350308hg38UCSC Ensembl
chr4:15351932..15351932hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17125517, nssv17139222
SamplesNA19239, HG00731
Known GenesC1QTNF7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5622260
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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