A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15204224



Internal ID21343027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:20225560..20225560hg38UCSC Ensembl
chr9:20225558..20225558hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3952102
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15204224
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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