A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3925631



Internal ID21345704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144824437..144824437hg38UCSC Ensembl
chr6:145145573..145145573hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15202602
SamplesHG002
Known GenesUTRN
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3925631
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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