A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17112439



Internal ID21454955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:239959643..239959703hg38UCSC Ensembl
chr2:240899060..240899120hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5570514
Supporting Variants
SamplesHG02011
Known GenesNDUFA10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17112439
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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