A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17129247



Internal ID21414633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15272566..15272631hg38UCSC Ensembl
chr3:15314073..15314138hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5575081
Supporting Variants
SamplesHG00513
Known GenesSH3BP5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17129247
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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