A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628171



Internal ID21576476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:120902665..120902665hg38UCSC Ensembl
chr10:122662177..122662177hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg386072
hg196072
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067573
SamplesHG03125
Known GenesMIR5694, WDR11
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628171
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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