A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3930771



Internal ID21350840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:120775664..120775664hg38UCSC Ensembl
chr10:122535176..122535176hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15191260
SamplesHG002
Known GenesMIR5694, WDR11-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3930771
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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