A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5601152



Internal ID21549796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56640464..56640780hg38UCSC Ensembl
chr11:56407940..56408256hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075368
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5601152
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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