A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637702



Internal ID21586007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:19939827..19939827hg38UCSC Ensembl
chr6:19940058..19940058hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17156050
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637702
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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