A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5602403



Internal ID21551061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76961782..76966775hg38UCSC Ensembl
chr11:76672826..76677819hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg384994
hg194994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076188
SamplesNA19238
Known GenesACER3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5602403
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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