A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3929145



Internal ID21349214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138650777..138650777hg38UCSC Ensembl
chr7:138335522..138335522hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381277
hg191277
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15203438
SamplesHG002
Known GenesSVOPL
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3929145
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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