A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5636558



Internal ID21584863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:206697..206697hg38UCSC Ensembl
chr7:206697..206697hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38382
hg19382
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155134
SamplesHG00732
Known GenesFAM20C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5636558
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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