A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3949090



Internal ID21369159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71752481..71752481hg38UCSC Ensembl
chr9:74367397..74367397hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15205550
SamplesHG002
Known GenesTMEM2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3949090
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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