A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3946708



Internal ID21366777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:107599844..107599844hg38UCSC Ensembl
chr1:108142466..108142466hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15185461
SamplesHG002
Known GenesVAV3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3946708
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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