A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3931341



Internal ID21351410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21057589..21057589hg38UCSC Ensembl
chr10:21346518..21346518hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15191562
SamplesHG002
Known GenesNEBL
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3931341
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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