A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3934325



Internal ID21354394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26955663..26955663hg38UCSC Ensembl
chr7:26995282..26995282hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15203781
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3934325
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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