A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17066931



Internal ID21457607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132404044..132404044hg38UCSC Ensembl
chr10:134217548..134217548hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5631549
Supporting Variants
SamplesHG02587
Known GenesPWWP2B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17066931
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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