A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3928196



Internal ID21348265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36703219..36703219hg38UCSC Ensembl
chr15:36995420..36995420hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15194579
SamplesHG002
Known GenesC15orf41
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3928196
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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