A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638862



Internal ID21587167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73563799..73563799hg38UCSC Ensembl
chr6:74273522..74273522hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155860
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638862
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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