A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093788



Internal ID21507702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45026649..45031607hg38UCSC Ensembl
chr15:45318847..45323805hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg384959
hg194959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5597796
Supporting Variants
SamplesNA20509
Known GenesSORD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093788
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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