A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3952763



Internal ID21372832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4149430..4149430hg38UCSC Ensembl
chr10:4191622..4191622hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15189532, nssv15189533
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3952763
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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