A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641230



Internal ID21589535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170508437..170508437hg38UCSC Ensembl
chr6:170817525..170817525hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381285
hg191285
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151410
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641230
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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