A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17060484



Internal ID21512098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13588980..13588980hg38UCSC Ensembl
chr1:13915475..13915475hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604800
Supporting Variants
SamplesNA24385
Known GenesPDPN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17060484
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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