A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3943613



Internal ID21363682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:159018226..159018226hg38UCSC Ensembl
chr7:158810917..158810917hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38656
hg19656
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15204314
SamplesHG002
Known GenesLINC00689
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3943613
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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