A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061228



Internal ID21487859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15859397..15866392hg38UCSC Ensembl
chr1:16185892..16192887hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg386996
hg196996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5570014
Supporting Variants
SamplesNA18534
Known GenesSPEN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061228
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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