A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591702



Internal ID21540280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76431283..76437506hg38UCSC Ensembl
chr11:76142327..76148550hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg386224
hg196224
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076160
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591702
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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