A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639860



Internal ID21588165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:70469094..70469094hg38UCSC Ensembl
chr9:73084010..73084010hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17162776, nssv17162775
SamplesHG03732, HG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639860
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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