A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639518



Internal ID21587823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74346380..74346380hg38UCSC Ensembl
chr9:76961296..76961296hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17162804
SamplesHG01505
Known GenesMIR6130
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639518
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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