A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090192



Internal ID21432750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52601768..52601768hg38UCSC Ensembl
chr15:52893965..52893965hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5647776
Supporting Variants
SamplesHG00731
Known GenesFAM214A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090192
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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