A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3942740



Internal ID21362809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140233596..140233596hg38UCSC Ensembl
chr7:139933396..139933396hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15203451
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3942740
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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