A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3925277



Internal ID21345346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149786210..149786210hg38UCSC Ensembl
chr6:150107346..150107346hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15202620
SamplesHG002
Known GenesPCMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3925277
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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