A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17138314



Internal ID21512071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15868481..15868546hg38UCSC Ensembl
chr3:15909988..15910053hg19UCSC 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 Variantsnsv5584010
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17138314
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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