A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3935527



Internal ID21355597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:39333608..39333608hg38UCSC Ensembl
chr5:39333710..39333710hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15201470
SamplesHG002
Known GenesC9
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3935527
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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