A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17107478



Internal ID21475870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10813740..10813828hg38UCSC Ensembl
chr2:10953866..10953954hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5584078
Supporting Variants
SamplesHG03486
Known GenesPDIA6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17107478
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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