A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17087737



Internal ID21456091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90974369..90974369hg38UCSC Ensembl
chr15:91517599..91517599hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5661541
Supporting Variants
SamplesHG02492
Known GenesPRC1, PRC1-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17087737
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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