A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025062



Internal ID21934405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56492866..56500420hg38UCSC Ensembl
chr11:56260342..56267896hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg387555
hg197555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583425
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025062
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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