A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17084357



Internal ID21447420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36703219..36703219hg38UCSC Ensembl
chr15:36995420..36995420hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5646436
Supporting Variants
SamplesHG00732
Known GenesC15orf41
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17084357
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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