A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3931759



Internal ID21351828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107727434..107727434hg38UCSC Ensembl
chr7:107367879..107367879hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38594
hg19594
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15203693
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3931759
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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