A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3951397



Internal ID21371466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15209429..15209429hg38UCSC Ensembl
chr10:15251428..15251428hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg383786
hg193786
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15191204
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3951397
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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