A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634732



Internal ID21583037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167997483..167997483hg38UCSC Ensembl
chr6:168398163..168398163hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153075
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634732
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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