A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17091500



Internal ID21439522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28377409..28377474hg38UCSC Ensembl
chr13:28951546..28951611hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5593376
Supporting Variants
SamplesHG00732
Known GenesFLT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17091500
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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