A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5592308



Internal ID21540889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74050711..74051276hg38UCSC Ensembl
chr11:73761756..73762321hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38566
hg19566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076051
SamplesNA19239
Known GenesC2CD3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5592308
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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