A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5602919



Internal ID21551579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62873847..62873932hg38UCSC Ensembl
chr11:62641319..62641404hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075740
SamplesHG00096
Known GenesSLC3A2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5602919
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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