A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5636883



Internal ID21585188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44883774..44883774hg38UCSC Ensembl
chr7:44923373..44923373hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17154452
SamplesHG00512
Known GenesPURB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5636883
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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