A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15205604



Internal ID21344406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109499103..109499103hg38UCSC Ensembl
chr9:112261383..112261383hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3951827
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15205604
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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