A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652644



Internal ID21600949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60982123..60982123hg38UCSC Ensembl
chr11:60749595..60749595hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075405
SamplesHG00731
Known GenesCD6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652644
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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