A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634002



Internal ID21582307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168264320..168264320hg38UCSC Ensembl
chr6:168665000..168665000hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38351
hg19351
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17144121
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634002
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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