A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5630185



Internal ID21578490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137018082..137018082hg38UCSC Ensembl
chr9:139912534..139912534hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38997
hg19997
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17160942
SamplesHG03732
Known GenesABCA2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5630185
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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