A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638344



Internal ID21586649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159898616..159898616hg38UCSC Ensembl
chr6:160319648..160319648hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17149684
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638344
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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