A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15205432



Internal ID21344239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134992443..134992443hg38UCSC Ensembl
chr9:137884289..137884289hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3947644
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15205432
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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