A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5595645



Internal ID21544252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31838448..31838975hg38UCSC Ensembl
chr11:31859995..31860522hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38528
hg19528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073957
SamplesNA19239
Known GenesDKFZp686K1684
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5595645
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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