A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15204283



Internal ID21343085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87867901..87867901hg38UCSC Ensembl
chr9:90482816..90482816hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3929305
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15204283
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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