A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5632370



Internal ID21580675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13547694..13547694hg38UCSC Ensembl
chr6:13547926..13547926hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17148633
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5632370
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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