A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5597653



Internal ID21546269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68169857..68169913hg38UCSC Ensembl
chr11:67937324..67937380hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075473
SamplesHG02011
Known GenesSUV420H1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5597653
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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