A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3938204



Internal ID21358274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114306315..114306315hg38UCSC Ensembl
chr10:116066074..116066074hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15189627
SamplesHG002
Known GenesAFAP1L2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3938204
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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