A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634331



Internal ID21582636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:55519555..55519555hg38UCSC Ensembl
chr7:55587248..55587248hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17152472
SamplesNA19239
Known GenesVOPP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634331
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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