A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584602



Internal ID21533144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1607726..1607812hg38UCSC Ensembl
chr11:1628956..1629042hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073749
SamplesNA19239
Known GenesKRTAP5-3, MOB2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584602
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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