A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639347



Internal ID21587652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63688231..63688231hg38UCSC Ensembl
chr6:64398132..64398132hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17142517
SamplesHG00731
Known GenesPHF3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639347
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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