A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035506



Internal ID21944849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:114472475..114478332hg38UCSC Ensembl
chr11:114343197..114349054hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg385858
hg195858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605781
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035506
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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