A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093182



Internal ID21478057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60366655..60367196hg38UCSC Ensembl
chr15:60658854..60659395hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38542
hg19542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591529
Supporting Variants
SamplesHG03486
Known GenesANXA2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093182
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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