A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3952102



Internal ID21372171
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15204224
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3952102
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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