A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925788



Internal ID22701015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56529189..56529449hg38UCSC Ensembl
chr11:56296665..56296925hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356374
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925788
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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