A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17069676



Internal ID21436062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32031868..32031868hg38UCSC Ensembl
chr10:32320796..32320796hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38364
hg19364
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5637046
Supporting Variants
SamplesHG00731
Known GenesKIF5B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17069676
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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