A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633727



Internal ID21582032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:134190878..134190878hg38UCSC Ensembl
chr7:133875630..133875630hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17145157, nssv17149547, nssv17143719
SamplesHG00512, HG00732, NA18939
Known GenesLRGUK
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633727
Frequency
Sample Size35
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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