A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5655842



Internal ID21604147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76916110..76916110hg38UCSC Ensembl
chr17:74912192..74912192hg19UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17084714
SamplesNA19983
Known GenesMGAT5B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5655842
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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