A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075368



Internal ID21456085
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 StatusS
Merged Variantsnsv5601152
Supporting Variants
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075368
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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