A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587907



Internal ID21536467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94885690..94890277hg38UCSC Ensembl
chr11:94618855..94623442hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg384588
hg194588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076854
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587907
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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