A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638689



Internal ID21586994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44616769..44616769hg38UCSC Ensembl
chr7:44656368..44656368hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17152956
SamplesNA19238
Known GenesOGDH
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638689
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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