A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3947481



Internal ID21367550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32031868..32031868hg38UCSC Ensembl
chr10:32320796..32320796hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38364
hg19364
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15191594
SamplesHG002
Known GenesKIF5B
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3947481
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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