A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638681



Internal ID21586986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:7274429..7274429hg38UCSC Ensembl
chr6:7274662..7274662hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17158159
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638681
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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