A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17059791



Internal ID21474006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:114902451..114902813hg38UCSC Ensembl
chr1:115445072..115445434hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38363
hg19363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5572176
Supporting Variants
SamplesHG03371
Known GenesSYCP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17059791
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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