A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5608600



Internal ID21556905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6698208..6698208hg38UCSC Ensembl
chr1:6758268..6758268hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17066394
SamplesHG02818
Known GenesDNAJC11
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5608600
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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