A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17066168



Internal ID21404743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63239685..63242474hg38UCSC Ensembl
chr1:63705356..63708145hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg382790
hg192790
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5579358
Supporting Variants
SamplesHG00512
Known GenesLINC00466
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17066168
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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