A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067563



Internal ID21463438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117126450..117126450hg38UCSC Ensembl
chr10:118885961..118885961hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5643875
Supporting Variants
SamplesHG03009
Known GenesKIAA1598
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067563
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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