A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17059640



Internal ID21438971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10274673..10274758hg38UCSC Ensembl
chr1:10334731..10334816hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5577217
Supporting Variants
SamplesHG00732
Known GenesKIF1B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17059640
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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